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 120

    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
    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
    nsv4984130copy number variation1nstd200human GRCh38 chr11: 1,716,430-1,797,665 , GRCh37.p13 chr11: 1,737,660-1,818,895 RPL36AP39, CTSD, 2 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
    nsv4599749copy number variation1nstd183human GRCh37 chr11: 1,760,556-1,841,827 , GRCh38.p12 chr11: 1,739,326-1,820,597 IFITM10, LOC105376517, 3 more genes
    nsv4527884copy number variation1nstd166human GRCh37.p13 chr11: 1,708,999-1,836,000 , GRCh38.p12 chr11: 1,687,769-1,814,770 CTSD, LOC390029, 5 more genes
    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
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv3959470insertion1nstd168human GRCh38 chr11: 1,769,144-1,798,305 , GRCh37.p13 chr11: 1,790,374-1,819,535 RPL36AP39, LOC105376517
    nsv3922910copy number variation1nstd102humanPathogenic NCBI36 chr11: 1,116,807-3,191,729 , GRCh38 chr11: 1,132,899-3,213,923 , GRCh37 chr11: 1,126,807-3,235,153 CARS1-AS1, TH, 69 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3919461copy number variation1nstd102humanPathogenic NCBI36 chr11: 1,515,185-3,338,575 , GRCh38 chr11: 1,537,379-3,360,769 , GRCh37 chr11: 1,558,609-3,381,999 C11orf21, SLC22A18AS, 67 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