Anthem Blue Cross and Blue Shield Virginia prior authorization, page 25

CPT code lookup

Each row is one code from the public prior authorization list. The description is the procedure or service name on that source row. This is not a coverage decision.

Prior authorization codes

Prior authorization codes
CodeDescriptionSource
81167BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full duplication/deletion analysis (ie, detection of large gene rearrangements)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81170ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) (eg, acquired imatinib tyrosine kinase inhibitor resistance), gene analysis, variants in the kinase domainVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81171AFF2 (ALF transcription elongation factor 2 [FMR2]) (eg, fragile X intellectual disability 2 [FRAXE]) gene analysis; evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81172AFF2 (ALF transcription elongation factor 2 [FMR2]) (eg, fragile X intellectual disability 2 [FRAXE]) gene analysis; characterization of alleles (eg, expanded size and methylaVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81173AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; full gene sequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81174AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; known familial variantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81175ASXL1 (additional sex combs like 1, transcriptional regulator) (eg, myelodysplastic syndrome, myeloproliferative neoplasms, chronic myelomonocytic leukemia), gene analysis; fuVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81176ASXL1 (additional sex combs like 1, transcriptional regulator) (eg, myelodysplastic syndrome, myeloproliferative neoplasms, chronic myelomonocytic leukemia), gene analysis; taVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81177ATN1 (atrophin 1) (eg, dentatorubral-pallidoluysian atrophy) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81178ATXN1 (ataxin 1) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81179ATXN2 (ataxin 2) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81180ATXN3 (ataxin 3) (eg, spinocerebellar ataxia, Machado-Joseph disease) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81181ATXN7 (ataxin 7) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81182ATXN8OS (ATXN8 opposite strand [non-protein coding]) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81183ATXN10 (ataxin 10) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81184CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81185CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; full gene sequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81186CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; known familial variantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81187CNBP (CCHC-type zinc finger nucleic acid binding protein) (eg, myotonic dystrophy type 2) gene analysis, evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81188CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; evaluation to detect abnormal (eg, expanded) allelesVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81189CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; full gene sequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81190CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81191NTRK1 (neurotrophic receptor tyrosine kinase 1) (eg, solid tumors) translocation analysisVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81192NTRK2 (neurotrophic receptor tyrosine kinase 2) (eg, solid tumors) translocation analysisVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81193NTRK3 (neurotrophic receptor tyrosine kinase 3) (eg, solid tumors) translocation analysisVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81194NTRK (neurotrophic-tropomyosin receptor tyrosine kinase 1, 2, and 3) (eg, solid tumors) translocation analysisVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 32 Original policy
81195Cytogenomic analysis, optical genome mappingVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81200Aspa (Aspartoacylase) (Eg, Canavan Disease) Gene Analysis, Common Variants (Eg, E285A, Y231X)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81201APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; full gene sequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81202APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; known familial variantsVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81203APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; duplication/deletion variantsVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81204AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; characterization of alleles (eg, expanded size or meVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81205Bckdhb (Branched-Chain Keto Acid Dehydrogenase E1, Beta Polypeptide) (Eg, Maple Syrup Urine Disease) Gene Analysis, Common Variants (Eg, R183P, G278S, E422X)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81206Bcr/Abl1 (T(9;22)) (Eg, Chronic Myelogenous Leukemia) Translocation Analysis; Major Breakpoint, Qualitative Or QuantitativeVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81207Bcr/Abl1 (T(9;22)) (Eg, Chronic Myelogenous Leukemia) Translocation Analysis; Minor Breakpoint, Qualitative Or QuantitativeVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81208Bcr/Abl1 (T(9;22)) (Eg, Chronic Myelogenous Leukemia) Translocation Analysis; Other Breakpoint, Qualitative Or QuantitativeVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81209Blm (Bloom Syndrome, Recq Helicase-Like) (Eg, Bloom Syndrome) Gene Analysis, 2281Del6Ins7 VariantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81210Braf (V-Raf Murine Sarcoma Viral Oncogene Homolog B1) (Eg, Colon Cancer), Gene Analysis, V600E VariantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81212BRCA1 (BRCA1, DNA repair associated), BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; 185delAG, 5385insC, 6174delT variantsVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81215BRCA1 (BRCA1, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; known familial variantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81216BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysisVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81217BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; known familial variantVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81218CEBPA (CCAAT/enhancer binding protein [C/EBP], alpha) (eg, acute myeloid leukemia), gene analysis, full gene sequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81219CALR (calreticulin) (eg, myeloproliferative disorders), gene analysis, common variants in exon 9Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81220Cftr (Cystic Fibrosis Transmembrane Conductance Regulator) (Eg, Cystic Fibrosis) Gene Analysis; Common Variants (Eg, Acmg/Acog Guidelines)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81221Cftr (Cystic Fibrosis Transmembrane Conductance Regulator) (Eg, Cystic Fibrosis) Gene Analysis; Known Familial VariantsVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81222Cftr (Cystic Fibrosis Transmembrane Conductance Regulator) (Eg, Cystic Fibrosis) Gene Analysis; Duplication/Deletion VariantsVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81223Cftr (Cystic Fibrosis Transmembrane Conductance Regulator) (Eg, Cystic Fibrosis) Gene Analysis; Full Gene SequenceVirginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81224Cftr (Cystic Fibrosis Transmembrane Conductance Regulator) (Eg, Cystic Fibrosis) Gene Analysis; Intron 8 Poly-T Analysis (Eg, Male Infertility)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy
81225Cyp2C19 (Cytochrome P450, Family 2, Subfamily C, Polypeptide 19) (Eg, Drug Metabolism), Gene Analysis, Common Variants (Eg, *2, *3, *4, *8, *17)Virginia HMO/EPO standard precertification/prior authorization requirements, Pg 33 Original policy

Sources

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The information provided on this page is for general informational purposes only and does not constitute billing, coding, or reimbursement advice. Nothing on this page should be relied upon as a substitute for clinician assessment, professional billing guidance, or as a definitive statement of any payor's billing requirements or policies.

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