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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922063copy number variation1nstd209human GRCh38 chr11: 1,554,280-1,554,389 , GRCh37.p13 chr11: 1,575,510-1,575,619 DUSP8
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5601770copy number variation1nstd207human GRCh38 chr11: 1,554,280-1,554,389 , GRCh37.p13 chr11: 1,575,510-1,575,619 DUSP8
    nsv5499592copy number variation1nstd206human GRCh38 chr11: 1,387,775-1,884,405 , GRCh37.p13 chr11: 1,409,005-1,905,635 , MOB2, 24 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
    nsv5332356translocation1nstd200human GRCh37 chr11: 1,587,052-1,587,052 , GRCh37 chr11: 1,587,116-1,587,116 , GRCh38.p12 chr11|NT_187657.1: 42,349-42,349 , GRCh38.p12 chr11|NT_187657.1: 42,413-42,413 , GRCh38.p12 chr11|NT_187584.1: 48,123-48,123 , GRCh38.p12 chr11: 1,565,822-1,565,822 , GRCh38.p12 chr11: 1,565,886-1,565,886 , GRCh38.p12 chr11|NT_187584.1: 48,059-48,059 DUSP8
    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
    nsv5245910copy number variation1nstd204human GRCh38.p13 chr11: 1,563,574-1,565,973 , GRCh37.p13 chr11: 1,584,804-1,587,203 DUSP8
    nsv4984126copy number variation1nstd200human GRCh38 chr11: 1,557,504-1,732,962 , GRCh37.p13 chr11: 1,578,734-1,754,192 DUSP8, KRTAP5-6, 10 more genes
    nsv4831140copy number variation1nstd200human GRCh37 chr11: 1,578,731-1,754,195 , GRCh38.p12 chr11: 1,557,501-1,732,965 , GRCh38.p12 chr11|NT_187584.1: 39,738-177,095 , GRCh38.p12 chr11|NT_187657.1: 34,028-206,711 LINC02708, KRTAP5-3, 10 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
    nsv4739385copy number variation1nstd199human GRCh37 chr11: 1,575,539-1,575,651 , GRCh38.p12 chr11|NT_187584.1: 36,546-36,658 , GRCh38.p12 chr11|NT_187657.1: 30,836-30,948 , GRCh38.p12 chr11: 1,554,309-1,554,421 DUSP8
    nsv4729545copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,436,158-2,321,134 , GRCh38.p12 chr11: 1,414,928-2,299,904 MIR4686, H19, 40 more genes
    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
    nsv4681514copy number variation2nstd102humanUncertain significance GRCh37 chr11: 612,625-2,193,840 , GRCh38.p12 chr11: 612,625-2,172,610 LINC02688, TNNI2, 74 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4480276mobile element insertion1nstd166human GRCh37.p13 chr11: 1,574,038-1,574,038 , GRCh38.p12 chr11: 1,552,808-1,552,808 , GRCh38.p12 chr11|NT_187584.1: 35,044-35,044 , GRCh38.p12 chr11|NT_187657.1: 29,335-29,335 DUSP8
    nsv4436605complex substitution1nstd102humanUncertain significance GRCh37 chr11: 870,446-1,857,751 , GRCh38.p12 chr11: 870,446-1,836,521 AP2A2, CTSD, 31 more genes
    nsv4436579complex substitution1nstd102humanUncertain significance GRCh37 chr11: 1,092,954-1,857,751 , GRCh38.p12 chr11: 1,138,209-1,836,521 CTSD, DUSP8, 24 more genes
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