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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6877156copy number variation1nstd229human GRCh38 chr9: 120,543,841-120,873,244 , GRCh37.p13 chr9: 123,306,119-123,635,522 AHCYP2, FBXW2, 6 more genes
    nsv6869300copy number variation1nstd229human GRCh38 chr9: 120,799,101-120,800,528 , GRCh37.p13 chr9: 123,561,379-123,562,806 B3GALT9
    nsv6866507copy number variation1nstd229human GRCh38 chr9: 120,797,208-120,797,286 , GRCh37.p13 chr9: 123,559,486-123,559,564 B3GALT9
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6443969copy number variation1nstd223human GRCh38 chr9: 120,799,101-120,800,528 , GRCh37.p13 chr9: 123,561,379-123,562,806 B3GALT9
    nsv6436955copy number variation1nstd223human GRCh38 chr9: 120,789,901-120,795,900 , GRCh37.p13 chr9: 123,552,179-123,558,178 FBXW2, B3GALT9
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137052copy number variation1nstd213human GRCh37 chr9: 123,200,000-125,840,001 , GRCh38.p12 chr9: 120,437,722-123,077,722 MEGF9, GGTA1, 61 more genes
    nsv5700528mobile element insertion1nstd211human GRCh38 chr9: 120,793,001-120,793,001 , GRCh37.p13 chr9: 123,555,279-123,555,279 B3GALT9, FBXW2
    nsv5480142copy number variation1nstd206human GRCh38 chr9: 120,793,878-120,793,967 , GRCh37.p13 chr9: 123,556,156-123,556,245 FBXW2, B3GALT9
    nsv5395548mobile element insertion1nstd206human GRCh38 chr9: 120,793,001-120,793,052 , GRCh37.p13 chr9: 123,555,279-123,555,330 FBXW2, B3GALT9
    nsv5373061translocation1nstd200human GRCh38 chr9: 120,800,528-120,800,528 , GRCh38 chr9: 120,799,101-120,799,101 , GRCh37.p13 chr9: 123,562,806-123,562,806 , GRCh37.p13 chr9: 123,561,379-123,561,379 B3GALT9
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983496copy number variation1nstd200human GRCh38 chr9: 120,791,509-120,792,705 , GRCh37.p13 chr9: 123,553,787-123,554,983 FBXW2, B3GALT9
    nsv4839479copy number variation1nstd200human GRCh37 chr9: 123,561,379-123,562,806 , GRCh38.p12 chr9: 120,799,101-120,800,528 B3GALT9
    nsv4833737copy number variation1nstd200human GRCh37 chr9: 123,553,787-123,554,983 , GRCh38.p12 chr9: 120,791,509-120,792,705 B3GALT9, FBXW2
    nsv4616049copy number variation1nstd183human GRCh37 chr9: 123,555,443-123,555,723 , GRCh38.p12 chr9: 120,793,165-120,793,445 B3GALT9, FBXW2
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