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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
    nsv5911176copy number variation1nstd209human GRCh38 chr11: 1,351,787-1,351,861 , GRCh37.p13 chr11: 1,373,017-1,373,091 LINC02689
    nsv5660911insertion1nstd207human GRCh38 chr11: 1,352,193-1,352,193 , GRCh37.p13 chr11: 1,373,423-1,373,423 LINC02689
    nsv5660638insertion1nstd207human GRCh38 chr11: 1,352,204-1,352,204 , GRCh37.p13 chr11: 1,373,434-1,373,434 LINC02689
    nsv5600010copy number variation1nstd207human GRCh38 chr11: 1,352,472-1,352,536 , GRCh37.p13 chr11: 1,373,702-1,373,766 LINC02689
    nsv5598457copy number variation1nstd207human GRCh38 chr11: 1,352,295-1,352,366 , GRCh37.p13 chr11: 1,373,525-1,373,596 LINC02689
    nsv5592665copy number variation1nstd207human GRCh38 chr11: 1,352,156-1,352,374 , GRCh37.p13 chr11: 1,373,386-1,373,604 LINC02689
    nsv5588516copy number variation1nstd207human GRCh38 chr11: 1,352,199-1,352,659 , GRCh37.p13 chr11: 1,373,429-1,373,889 LINC02689
    nsv5511048copy number variation1nstd206human GRCh38 chr11: 1,358,420-1,358,544 , GRCh37.p13 chr11: 1,379,650-1,379,774 LINC02689
    nsv5509656copy number variation1nstd206human GRCh38 chr11: 1,355,176-1,355,685 , GRCh37.p13 chr11: 1,376,406-1,376,915 LINC02689
    nsv5504454copy number variation1nstd206human GRCh38 chr11: 1,204,311-1,445,084 , GRCh37.p13 chr11: 1,225,541-1,466,314 , BRSK2, 7 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
    nsv5256220copy number variation1nstd204human GRCh38.p13 chr11: 1,018,601-1,642,300 , GRCh37.p13 chr11: 1,018,601-1,663,530 , KRTAP5-1, 21 more genes
    nsv5247913copy number variation1nstd204human GRCh37.p13 chr11: 1,315,731-1,531,430 , GRCh38.p13 chr11: 1,294,501-1,510,200 , BRSK2, 6 more genes
    nsv4984122copy number variation1nstd200human GRCh38 chr11: 1,355,118-1,355,793 , GRCh37.p13 chr11: 1,376,348-1,377,023 LINC02689
    nsv4984121copy number variation1nstd200human GRCh38 chr11: 1,302,941-1,410,091 , GRCh37.p13 chr11: 1,324,171-1,431,321 , TOLLIP-DT, 3 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
    nsv4734930copy number variation1nstd199human GRCh37 chr11: 1,373,188-1,373,608 , GRCh38.p12 chr11: 1,351,958-1,352,378 LINC02689
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 more genes
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