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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139004insertion1nstd232human GRCh37.p13 chr9: 114,900,518-114,900,518 , GRCh38.p12 chr9: 112,138,238-112,138,238 SUSD1, RNU6-855P
    nsv7077621inversion1nstd229human GRCh38 chr9: 112,105,538-112,337,285 , GRCh37.p13 chr9: 114,867,818-115,099,565 HSPE1P28, RPL29P20, 6 more genes
    nsv7061375inversion1nstd229human GRCh38 chr9: 111,842,382-112,467,830 , GRCh37.p13 chr9: 114,604,662-115,230,110 RPL29P20, RNU6-710P, 13 more genes
    nsv6877814copy number variation1nstd229human GRCh38 chr9: 112,134,340-112,138,270 , GRCh37.p13 chr9: 114,896,620-114,900,550 RNU6-855P, SUSD1
    nsv6874632copy number variation1nstd229human GRCh38 chr9: 112,173,201-112,215,000 , GRCh37.p13 chr9: 114,935,481-114,977,280 RPL29P20, SUSD1
    nsv6873547copy number variation1nstd229human GRCh38 chr9: 112,134,108-112,172,761 , GRCh37.p13 chr9: 114,896,388-114,935,041 RPL29P20, RNU6-855P, 1 more genes
    nsv6872720copy number variation1nstd229human GRCh38 chr9: 112,037,459-112,041,555 , GRCh37.p13 chr9: 114,799,739-114,803,835 SUSD1, LINC02977
    nsv6871311copy number variation1nstd229human GRCh38 chr9: 112,132,901-112,135,200 , GRCh37.p13 chr9: 114,895,181-114,897,480 SUSD1
    nsv6870928copy number variation1nstd229human GRCh38 chr9: 112,149,386-112,152,603 , GRCh37.p13 chr9: 114,911,666-114,914,883 SUSD1
    nsv6870794copy number variation1nstd229human GRCh38 chr9: 112,140,079-112,140,377 , GRCh37.p13 chr9: 114,902,359-114,902,657 SUSD1
    nsv6869750copy number variation1nstd229human GRCh38 chr9: 112,064,020-112,070,583 , GRCh37.p13 chr9: 114,826,300-114,832,863 SUSD1
    nsv6869234copy number variation1nstd229human GRCh38 chr9: 112,064,618-112,064,663 , GRCh37.p13 chr9: 114,826,898-114,826,943 SUSD1
    nsv6862813copy number variation1nstd229human GRCh38 chr9: 111,987,261-112,081,659 , GRCh37.p13 chr9: 114,749,541-114,843,939 RNU6-710P, LINC02977, 1 more genes
    nsv6861240copy number variation1nstd229human GRCh38 chr9: 111,949,167-112,127,208 , GRCh37.p13 chr9: 114,711,447-114,889,488 LINC02977, SUSD1, 1 more genes
    nsv6860532copy number variation1nstd229human GRCh38 chr9: 112,128,319-112,133,925 , GRCh37.p13 chr9: 114,890,599-114,896,205 SUSD1
    nsv6858844copy number variation1nstd229human GRCh38 chr9: 112,049,277-112,060,734 , GRCh37.p13 chr9: 114,811,557-114,823,014 SUSD1
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633388copy number variation1nstd224human GRCh37 chr9: 114,888,773-114,905,753 , GRCh38.p12 chr9: 112,126,493-112,143,473 RNU6-855P, SUSD1
    nsv6575127inversion1nstd223human GRCh38 chr9: 112,097,052-112,097,652 , GRCh37.p13 chr9: 114,859,332-114,859,932 SUSD1
    nsv6574631inversion1nstd223human GRCh38 chr9: 112,142,993-112,144,177 , GRCh37.p13 chr9: 114,905,273-114,906,457 SUSD1
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