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CPT®
0267U

CPT® Code 0267U

Official Description

Rare constitutional and other heritable disorders, identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping and whole genome sequencing

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Short Descr RARE DO ID OPT GEN MAPG&SEQ
Medium Descr RARE DO ID VARIATIONS OPT GEN MAP&WHL GEN SEQ
Long Descr Rare constitutional and other heritable disorders, identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping and whole genome sequencing
CLIA Waived (QW) No
APC Status Indicator Service Paid under Fee Schedule or Payment System other than OPPS
Berenson-Eggers TOS (BETOS) none
MUE 1
Date
Action
Notes
2022-01-01 Added First appearance in codebook.
2021-10-01 Added Code added.
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