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| Short Descr | RARE DS ID OPT GENOME MAPG | Medium Descr | RARE DS ID VRTJ INVRJ INSJ TLCJ OPT GENOME MAPG | Long Descr | Rare diseases (constitutional/heritable disorders), identification of copy number variations, inversions, insertions, translocations, and other structural variants by optical genome mapping | 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 |
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| 2025-01-01 | Added | First appearance in codebook. |
| 2024-07-01 | Added | Code added. |
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