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Items: 1 to 20 of 303

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5910466copy number variation1nstd209human GRCh38 chr11: 2,161,592-2,161,830 , GRCh37.p13 chr11: 2,182,822-2,183,060 INS-IGF2, INS
    nsv5659617insertion1nstd207human GRCh38 chr11: 2,141,511-2,141,511 , GRCh37.p13 chr11: 2,162,741-2,162,741 IGF2, IGF2-AS, 1 more genes
    nsv5657418insertion1nstd207human GRCh38 chr11: 2,127,161-2,127,161 , GRCh37.p13 chr11: 2,148,391-2,148,391 IGF2, INS-IGF2
    nsv5654765insertion1nstd207human GRCh38 chr11: 2,161,592-2,161,592 , GRCh37.p13 chr11: 2,182,822-2,182,822 INS-IGF2, INS
    nsv5651768insertion1nstd207human GRCh38 chr11: 2,137,536-2,137,536 , GRCh37.p13 chr11: 2,158,766-2,158,766 IGF2, INS-IGF2
    nsv5650794insertion1nstd207human GRCh38 chr11: 2,145,100-2,145,100 , GRCh37.p13 chr11: 2,166,330-2,166,330 IGF2, IGF2-AS, 1 more genes
    nsv5647141insertion1nstd207human GRCh38 chr11: 2,127,170-2,127,170 , GRCh37.p13 chr11: 2,148,400-2,148,400 IGF2, INS-IGF2
    nsv5645385insertion3nstd207human GRCh38 chr11: 2,161,579-2,161,579 , GRCh37.p13 chr11: 2,182,809-2,182,809 INS, INS-IGF2
    nsv5512635copy number variation1nstd206human GRCh38 chr11: 2,132,065-2,132,140 , GRCh37.p13 chr11: 2,153,295-2,153,370 MIR483, IGF2, 1 more genes
    nsv5500844copy number variation1nstd206human GRCh38 chr11: 2,134,488-2,135,135 , GRCh37.p13 chr11: 2,155,718-2,156,365 MIR483, INS-IGF2, 1 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5259948copy number variation1nstd204human GRCh38.p13 chr11: 1,804,001-2,194,300 , GRCh37.p13 chr11: 1,825,231-2,215,530 H19, INS, 20 more genes
    nsv5255919copy number variation1nstd204human GRCh38.p13 chr11: 2,123,001-2,130,400 , GRCh37.p13 chr11: 2,144,231-2,151,630 IGF2, INS-IGF2
    nsv5249142copy number variation1nstd204human GRCh38.p13 chr11: 2,152,405-2,153,704 , GRCh37.p13 chr11: 2,173,635-2,174,934 INS-IGF2
    nsv5245737copy number variation1nstd204human GRCh38.p13 chr11: 2,140,561-2,143,468 , GRCh37.p13 chr11: 2,161,791-2,164,698 IGF2, INS-IGF2, 1 more genes
    nsv5128065mobile element insertion1nstd203human GRCh38 chr11: 2,146,210-2,146,225 , GRCh37.p13 chr11: 2,167,440-2,167,455 IGF2, IGF2-AS, 1 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4753822insertion1nstd199human GRCh37 chr11: 2,182,803-2,182,803 , GRCh38.p12 chr11: 2,161,573-2,161,573 INS, INS-IGF2
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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