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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924732copy number variation1nstd209human GRCh38 chr9: 137,217,032-137,217,082 , GRCh37.p13 chr9: 140,111,484-140,111,534 NDOR1
    nsv5916047copy number variation1nstd209human GRCh38 chr9: 137,218,332-137,218,573 , GRCh37.p13 chr9: 140,112,784-140,113,025 NDOR1, RNF208
    nsv5632167insertion1nstd207human GRCh38 chr9: 137,217,032-137,217,032 , GRCh37.p13 chr9: 140,111,484-140,111,484 NDOR1
    nsv5602572copy number variation1nstd207human GRCh38 chr9: 137,217,032-137,217,082 , GRCh37.p13 chr9: 140,111,484-140,111,534 NDOR1
    nsv5492970copy number variation1nstd206human GRCh38 chr9: 137,218,334-137,218,574 , GRCh37.p13 chr9: 140,112,786-140,113,026 RNF208, NDOR1
    nsv5491629copy number variation1nstd206human GRCh38 chr9: 137,205,774-137,227,901 , GRCh37.p13 chr9: 140,100,226-140,122,353 NDOR1, CYSRT1, 3 more genes
    nsv5490912copy number variation1nstd206human GRCh38 chr9: 137,209,880-137,210,670 , GRCh37.p13 chr9: 140,104,332-140,105,122 NDOR1
    nsv5481732copy number variation1nstd206human GRCh38 chr9: 137,215,306-137,215,373 , GRCh37.p13 chr9: 140,109,758-140,109,825 NDOR1
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5373217translocation1nstd200human GRCh38 chr9: 137,218,334-137,218,334 , GRCh38 chr9: 137,218,574-137,218,574 , GRCh37.p13 chr9: 140,113,026-140,113,026 , GRCh37.p13 chr9: 140,112,786-140,112,786 NDOR1, RNF208
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 more genes
    nsv4985885copy number variation1nstd200human GRCh38 chr9: 137,194,542-137,210,900 , GRCh37.p13 chr9: 140,088,994-140,105,352 TMEM203, NDOR1, 1 more genes
    nsv4832950copy number variation1nstd200human GRCh37 chr9: 140,088,994-140,105,352 , GRCh38.p12 chr9: 137,194,542-137,210,900 TPRN, TMEM203, 1 more genes
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4743038copy number variation1nstd199human GRCh37 chr9: 140,111,539-140,111,590 , GRCh38.p12 chr9: 137,217,087-137,217,138 NDOR1
    nsv4728942copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,776,707-140,234,193 , GRCh38.p12 chr9: 136,882,255-137,339,741 GRIN1, CYSRT1, 42 more genes
    nsv4728051copy number variation1nstd197human GRCh38.p12 chr9: 137,212,503-137,236,416 , GRCh37 chr9: 140,106,955-140,130,868 NDOR1, SLC34A3, 3 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683512copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,033,919-140,729,425 , GRCh38.p12 chr9: 137,139,467-137,834,973 CIMIP2A, ENTPD8, 34 more genes
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