Anthem Blue Cross and Blue Shield Nevada prior authorization, page 40

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
78608Brain Imaging, Positron Emission Tomography (Pet); Metabolic EvaluationNevada Prior Authorization List, Pg 87 Original policy
78609Brain Imaging, Positron Emission Tomography (Pet); Perfusion EvaluationNevada Prior Authorization List, Pg 87 Original policy
78811Positron emission tomography (PET) imaging; limited area (eg, chest, head/neck)Nevada Prior Authorization List, Pg 87 Original policy
78812Positron emission tomography (PET) imaging; skull base to mid-thighNevada Prior Authorization List, Pg 87 Original policy
78813Positron emission tomography (PET) imaging; whole bodyNevada Prior Authorization List, Pg 87 Original policy
78814Positron emission tomography (PET) with concurrently acquired computed tomography (CT) for attenuation correction and anNevada Prior Authorization List, Pg 87 Original policy
78815Positron emission tomography (PET) with concurrently acquired computed tomography (CT) for attenuation correction and anNevada Prior Authorization List, Pg 87 Original policy
78816Positron emission tomography (PET) with concurrently acquired computed tomography (CT) for attenuation correction and anNevada Prior Authorization List, Pg 87 Original policy
79101Radiopharmaceutical Therapy, By Intravenous AdministrationNevada Prior Authorization List, Pg 87 Original policy
79403Radiopharmaceutical Therapy, Radiolabeled Monoclonal Antibody By Intravenous InfusionNevada Prior Authorization List, Pg 87 Original policy
81120IDH1 (isocitrate dehydrogenase 1 [NADP+], soluble) (eg, glioma), common variants (eg, R132H, R132C)Nevada Prior Authorization List, Pg 87 Original policy
81121IDH2 (isocitrate dehydrogenase 2 [NADP+], mitochondrial) (eg, glioma), common variants (eg, R140W, R172M)Nevada Prior Authorization List, Pg 87 Original policy
81161DMD (dystrophin) (eg, Duchenne/Becker muscular dystrophy) deletion analysis, and duplication analysis, if performedNevada Prior Authorization List, Pg 87 Original policy
81162BRCA1 (BRCA1, DNA repair associated), BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysis and full duplicatioNevada Prior Authorization List, Pg 87 Original policy
81163BRCA1 (BRCA1, DNA repair associated), BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysisNevada Prior Authorization List, Pg 87 Original policy
81164BRCA1 (BRCA1, DNA repair associated), BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full duplication/deletion analysis (ie, deNevada Prior Authorization List, Pg 87 Original policy
81165BRCA1 (BRCA1, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full sequence analysisNevada Prior Authorization List, Pg 87 Original policy
81166BRCA1 (BRCA1, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full duplication/deletion analysis (ie, detection of large gene rearrangements)Nevada Prior Authorization List, Pg 87 Original policy
81167BRCA2 (BRCA2, DNA repair associated) (eg, hereditary breast and ovarian cancer) gene analysis; full duplication/deletion analysis (ie, detection of large gene rearrangements)Nevada Prior Authorization List, Pg 87 Original policy
81170ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) (eg, acquired imatinib tyrosine kinase inhibitor resistance), gene analysis, variants in the kinase domainNevada Prior Authorization List, Pg 87 Original policy
81171AFF2 (ALF transcription elongation factor 2 [FMR2]) (eg, fragile X intellectual disability 2 [FRAXE]) gene analysis; evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 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 methylaNevada Prior Authorization List, Pg 88 Original policy
81173AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; full gene sequenceNevada Prior Authorization List, Pg 88 Original policy
81174AR (androgen receptor) (eg, spinal and bulbar muscular atrophy, Kennedy disease, X chromosome inactivation) gene analysis; known familial variantNevada Prior Authorization List, Pg 88 Original policy
81175ASXL1 (additional sex combs like 1, transcriptional regulator) (eg, myelodysplastic syndrome, myeloproliferative neoplasms, chronic myelomonocytic leukemia), gene analysis; fuNevada Prior Authorization List, Pg 88 Original policy
81176ASXL1 (additional sex combs like 1, transcriptional regulator) (eg, myelodysplastic syndrome, myeloproliferative neoplasms, chronic myelomonocytic leukemia), gene analysis; taNevada Prior Authorization List, Pg 88 Original policy
81177ATN1 (atrophin 1) (eg, dentatorubral-pallidoluysian atrophy) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81178ATXN1 (ataxin 1) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81179ATXN2 (ataxin 2) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81180ATXN3 (ataxin 3) (eg, spinocerebellar ataxia, Machado-Joseph disease) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81181ATXN7 (ataxin 7) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81182ATXN8OS (ATXN8 opposite strand [non-protein coding]) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81183ATXN10 (ataxin 10) (eg, spinocerebellar ataxia) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81184CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81185CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; full gene sequenceNevada Prior Authorization List, Pg 88 Original policy
81186CACNA1A (calcium voltage-gated channel subunit alpha1 A) (eg, spinocerebellar ataxia) gene analysis; known familial variantNevada Prior Authorization List, Pg 88 Original policy
81187CNBP (CCHC-type zinc finger nucleic acid binding protein) (eg, myotonic dystrophy type 2) gene analysis, evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81188CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; evaluation to detect abnormal (eg, expanded) allelesNevada Prior Authorization List, Pg 88 Original policy
81189CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; full gene sequenceNevada Prior Authorization List, Pg 88 Original policy
81190CSTB (cystatin B) (eg, Unverricht-Lundborg disease) gene analysis; known familial variant(s)Nevada Prior Authorization List, Pg 88 Original policy
81191NTRK1 (neurotrophic receptor tyrosine kinase 1) (eg, solid tumors) translocation analysisNevada Prior Authorization List, Pg 88 Original policy
81192NTRK2 (neurotrophic receptor tyrosine kinase 2) (eg, solid tumors) translocation analysisNevada Prior Authorization List, Pg 88 Original policy
81193NTRK3 (neurotrophic receptor tyrosine kinase 3) (eg, solid tumors) translocation analysisNevada Prior Authorization List, Pg 88 Original policy
81194NTRK (neurotrophic-tropomyosin receptor tyrosine kinase 1, 2, and 3) (eg, solid tumors) translocation analysisNevada Prior Authorization List, Pg 88 Original policy
81195Cytogenomic analysis, optical genome mappingNevada Prior Authorization List, Pg 88 Original policy
81200Aspa (Aspartoacylase) (Eg, Canavan Disease) Gene Analysis, Common Variants (Eg, E285A, Y231X)Nevada Prior Authorization List, Pg 89 Original policy
81201APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; full gene sequenceNevada Prior Authorization List, Pg 89 Original policy
81202APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; known familial variantsNevada Prior Authorization List, Pg 89 Original policy
81203APC (adenomatous polyposis coli) (eg, familial adenomatosis polyposis [FAP], attenuated FAP) gene analysis; duplication/deletion variantsNevada Prior Authorization List, Pg 89 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 meNevada Prior Authorization List, Pg 89 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.

Payor agreements, fee schedules, and billing policies vary and are subject to change. Before submitting any claims related to maternity care services, including claims affected by the 2027 CPT code revisions, please consult the applicable payor agreements, coverage policies, and billing guidelines to confirm current requirements for their specific payor contracts.

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