U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 219

    loading data ...

    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
    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
    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
    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
    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
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center