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Items: 1 to 20 of 749

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130062insertion1nstd186human GRCh37 chr13: 110,857,832-110,857,837 , GRCh38.p12 chr13: 110,205,485-110,205,490 COL4A1
    nsv6123275copy number variation1nstd186human GRCh37 chr13: 110,874,837-110,875,142 , GRCh38.p12 chr13: 110,222,490-110,222,795 COL4A1
    nsv6121777copy number variation1nstd186human GRCh37 chr13: 110,812,508-110,812,806 , GRCh38.p12 chr13: 110,160,161-110,160,459 COL4A1
    nsv5980390copy number variation1nstd102humanUncertain significance GRCh37 chr13: 110,802,791-110,959,290 , GRCh38.p12 chr13: 110,150,444-110,306,943 COL4A1, COL4A2
    nsv5977299insertion1nstd209human GRCh38 chr13: 110,252,655-110,252,655 , GRCh37.p13 chr13: 110,905,002-110,905,002 COL4A1
    nsv5977000insertion1nstd209human GRCh38 chr13: 110,201,270-110,201,270 , GRCh37.p13 chr13: 110,853,617-110,853,617 COL4A1
    nsv5975198insertion1nstd209human GRCh38 chr13: 110,222,771-110,222,771 , GRCh37.p13 chr13: 110,875,118-110,875,118 COL4A1
    nsv5941204copy number variation1nstd209human GRCh38 chr13: 110,160,144-110,160,458 , GRCh37.p13 chr13: 110,812,491-110,812,805 COL4A1
    nsv5940231copy number variation1nstd209human GRCh38 chr13: 110,219,816-110,219,877 , GRCh37.p13 chr13: 110,872,163-110,872,224 COL4A1
    nsv5937994copy number variation1nstd209human GRCh38 chr13: 110,222,471-110,222,794 , GRCh37.p13 chr13: 110,874,818-110,875,141 COL4A1
    nsv5937609copy number variation1nstd209human GRCh38 chr13: 110,253,304-110,253,458 , GRCh37.p13 chr13: 110,905,651-110,905,805 COL4A1
    nsv5935256copy number variation1nstd209human GRCh38 chr13: 110,170,953-110,172,091 , GRCh37.p13 chr13: 110,823,300-110,824,438 COL4A1
    nsv5928725copy number variation1nstd209human GRCh38 chr13: 110,253,752-110,253,804 , GRCh37.p13 chr13: 110,906,099-110,906,151 COL4A1
    nsv5860724copy number variation1nstd209human GRCh38 chr13: 110,266,688-110,267,687 , GRCh37.p13 chr13: 110,919,035-110,920,034 COL4A1
    nsv5712566mobile element insertion2nstd211human GRCh38 chr13: 110,210,279-110,210,279 , GRCh37.p13 chr13: 110,862,626-110,862,626 COL4A1
    nsv5696517mobile element insertion2nstd211human GRCh38 chr13: 110,205,485-110,205,485 , GRCh37.p13 chr13: 110,857,832-110,857,832 COL4A1
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5661765insertion1nstd207human GRCh38 chr13: 110,255,826-110,255,826 , GRCh37.p13 chr13: 110,908,173-110,908,173 COL4A1
    nsv5660554insertion1nstd207human GRCh38 chr13: 110,252,655-110,252,655 , GRCh37.p13 chr13: 110,905,002-110,905,002 COL4A1
    nsv5660491insertion2nstd207human GRCh38 chr13: 110,252,788-110,252,788 , GRCh37.p13 chr13: 110,905,135-110,905,135 COL4A1
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