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 103

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6906583copy number variation1nstd229human GRCh38 chr11: 58,777,503-58,909,891 , GRCh37.p13 chr11: 58,544,976-58,677,364 GLYATL2, TMA16P1, 2 more genes
    nsv6904323copy number variation1nstd229human GRCh38 chr11: 58,827,321-59,212,101 , GRCh37.p13 chr11: 58,594,794-58,979,574 LOC100422399, LOC105369315, 14 more genes
    nsv6473679copy number variation1nstd223human GRCh38 chr11: 58,887,801-58,889,400 , GRCh37.p13 chr11: 58,655,274-58,656,873 GLYATL1P2, GLYATL2
    nsv6470226copy number variation1nstd223human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 LOC105369315, DTX4, 29 more genes
    nsv6463149copy number variation1nstd223human GRCh38 chr11: 58,777,503-58,909,891 , GRCh37.p13 chr11: 58,544,976-58,677,364 GLYATL2, GLYATL1P2, 2 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5918762copy number variation1nstd209human GRCh38 chr11: 58,832,259-58,997,961 , GRCh37.p13 chr11: 58,599,732-58,765,434 GLYATL1, GLYATL2, 5 more genes
    nsv5908645copy number variation1nstd209human GRCh38 chr11: 58,846,467-59,011,722 , GRCh37.p13 chr11: 58,613,940-58,779,195 GLYATL1, GLYATL2, 5 more genes
    nsv5503704copy number variation1nstd206human GRCh38 chr11: 58,888,274-58,888,362 , GRCh37.p13 chr11: 58,655,747-58,655,835 GLYATL1P2, GLYATL2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv4984975copy number variation1nstd200human GRCh38 chr11: 58,777,503-58,909,891 , GRCh37.p13 chr11: 58,544,976-58,677,364 GLYATL2, GLYATL1P2, 2 more genes
    nsv4984973copy number variation1nstd200human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 GLYATL1P4, LOC283194, 29 more genes
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 58,602,498-59,091,934 , GRCh38.p12 chr11: 58,835,025-59,324,461 LOC100422398, LOC643709, 20 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