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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974895inversion1nstd209human GRCh38 chr7: 4,776,436-4,777,685 , GRCh37.p13 chr7: 4,816,067-4,817,316 AP5Z1
    nsv5561992sequence alteration1nstd206human GRCh37.p13 chr7: 4,815,023-4,925,060 , GRCh38 chr7: 4,775,392-4,885,429 AP5Z1, RADIL, 4 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5465505copy number variation1nstd206human GRCh38 chr7: 4,763,289-4,870,637 , GRCh37.p13 chr7: 4,802,920-4,910,268 AP5Z1, RADIL, 5 more genes
    nsv5456142copy number variation1nstd206human GRCh38 chr7: 4,776,534-4,785,522 , GRCh37.p13 chr7: 4,816,165-4,825,153 AP5Z1
    nsv5455631copy number variation1nstd206human GRCh38 chr7: 4,786,121-4,789,076 , GRCh37.p13 chr7: 4,825,752-4,828,707 MIR4656, AP5Z1
    nsv5311319copy number variation1nstd204human GRCh37.p13 chr7: 4,825,747-4,828,709 , GRCh38.p13 chr7: 4,786,116-4,789,078 MIR4656, AP5Z1
    nsv5309577copy number variation1nstd204human GRCh38.p13 chr7: 4,780,965-4,792,331 , GRCh37.p13 chr7: 4,820,596-4,831,962 AP5Z1, MIR4656
    nsv5239555copy number variation1nstd204human GRCh38.p13 chr7: 4,780,382-4,792,609 , GRCh37.p13 chr7: 4,820,013-4,832,240 AP5Z1, MIR4656
    nsv5224724copy number variation1nstd204human GRCh38.p13 chr7: 4,786,082-4,789,535 , GRCh37.p13 chr7: 4,825,713-4,829,166 MIR4656, AP5Z1
    nsv4949845copy number variation1nstd200human GRCh38 chr7: 4,786,121-4,789,076 , GRCh37.p13 chr7: 4,825,752-4,828,707 AP5Z1, MIR4656
    nsv4949844copy number variation1nstd200human GRCh38 chr7: 4,776,184-4,782,910 , GRCh37.p13 chr7: 4,815,815-4,822,541 AP5Z1
    nsv4818512copy number variation1nstd200human GRCh37 chr7: 4,825,752-4,828,707 , GRCh38.p12 chr7: 4,786,121-4,789,076 AP5Z1, MIR4656
    nsv4818511copy number variation1nstd200human GRCh37 chr7: 4,816,162-4,825,153 , GRCh38.p12 chr7: 4,776,531-4,785,522 AP5Z1
    nsv4818510copy number variation1nstd200human GRCh37 chr7: 4,815,815-4,822,541 , GRCh38.p12 chr7: 4,776,184-4,782,910 AP5Z1
    nsv4729642copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,457,599-5,138,409 , GRCh38.p12 chr7: 4,417,968-5,098,778 LOC105375134, MIR4656, 15 more genes
    nsv4729297copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,733,073-5,157,165 , GRCh38.p12 chr7: 4,693,442-5,117,534 RBAKDN, RNF216P1, 13 more genes
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4613860copy number variation1nstd183human GRCh37 chr7: 4,809,219-4,851,285 , GRCh38.p12 chr7: 4,769,588-4,811,654 FOXK1, AP5Z1, 2 more genes
    nsv4456924copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,807,055-4,930,807 , GRCh38.p12 chr7: 4,767,424-4,891,176 RADIL, MIR4656, 6 more genes
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