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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705080mobile element insertion1nstd211human GRCh38 chr9: 99,928,529-99,928,529 , GRCh37.p13 chr9: 102,690,811-102,690,811 STX17
    nsv5697871mobile element insertion1nstd211human GRCh38 chr9: 99,908,400-99,908,400 , GRCh37.p13 chr9: 102,670,682-102,670,682 STX17
    nsv5543526insertion1nstd206human GRCh38 chr9: 99,934,255-99,934,290 , GRCh37.p13 chr9: 102,696,537-102,696,572 STX17
    nsv5402440mobile element insertion1nstd206human GRCh38 chr9: 99,908,400-99,908,451 , GRCh37.p13 chr9: 102,670,682-102,670,733 STX17
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372879translocation1nstd200human GRCh38 chr9: 99,961,830-99,961,830 , GRCh38 chr9: 99,979,161-99,979,161 , GRCh37.p13 chr9: 102,724,112-102,724,112 , GRCh37.p13 chr9: 102,741,443-102,741,443 STX17, ERP44
    nsv5372878translocation1nstd200human GRCh38 chr9: 99,930,558-99,930,558 , GRCh38 chr9: 99,931,226-99,931,226 , GRCh37.p13 chr9: 102,693,508-102,693,508 , GRCh37.p13 chr9: 102,692,840-102,692,840 STX17
    nsv5135924mobile element insertion1nstd203human GRCh38 chr9: 99,934,239-99,934,255 , GRCh37.p13 chr9: 102,696,521-102,696,537 STX17
    nsv4982761copy number variation1nstd200human GRCh38 chr9: 99,933,686-99,937,865 , GRCh37.p13 chr9: 102,695,968-102,700,147 STX17
    nsv4982760copy number variation1nstd200human GRCh38 chr9: 99,929,258-99,933,540 , GRCh37.p13 chr9: 102,691,540-102,695,822 STX17
    nsv4982759copy number variation1nstd200human GRCh38 chr9: 99,909,515-99,910,617 , GRCh37.p13 chr9: 102,671,797-102,672,899 STX17
    nsv4824227copy number variation1nstd200human GRCh37 chr9: 102,734,165-102,735,622 , GRCh38.p12 chr9: 99,971,883-99,973,340 STX17
    nsv4824226copy number variation1nstd200human GRCh37 chr9: 102,687,287-102,687,680 , GRCh38.p12 chr9: 99,925,005-99,925,398 STX17
    nsv4824225copy number variation1nstd200human GRCh37 chr9: 102,671,797-102,672,899 , GRCh38.p12 chr9: 99,909,515-99,910,617 STX17
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4491579mobile element insertion1nstd166human GRCh37.p13 chr9: 102,734,355-102,734,355 , GRCh38.p12 chr9: 99,972,073-99,972,073 STX17
    nsv4486494mobile element insertion1nstd166human GRCh37.p13 chr9: 102,696,521-102,696,521 , GRCh38.p12 chr9: 99,934,239-99,934,239 STX17
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
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