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 85

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6910053copy number variation1nstd229human GRCh38 chr11: 62,363,901-63,050,100 , GRCh37.p13 chr11: 62,131,373-62,817,572 MIR6747, TMEM179B, 54 more genes
    nsv6908114copy number variation1nstd229human GRCh38 chr11: 62,593,901-63,028,400 , GRCh37.p13 chr11: 62,361,373-62,795,872 GANAB, SLC22A6, 44 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904565copy number variation1nstd229human GRCh38 chr11: 62,240,001-63,046,600 , GRCh37.p13 chr11: 62,007,473-62,814,072 RCC2P6, SNORD26, 58 more genes
    nsv6903779copy number variation1nstd229human GRCh38 chr11: 62,796,669-62,913,409 , GRCh37.p13 chr11: 62,564,141-62,680,881 SNORD30, STX5-DT, 16 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6900187copy number variation1nstd229human GRCh38 chr11: 62,838,248-62,866,261 , GRCh37.p13 chr11: 62,605,720-62,633,733 WDR74, SNORD30, 10 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
    nsv6131999copy number variation1nstd213human GRCh37 chr11: 62,579,390-62,707,802 , GRCh38.p12 chr11: 62,811,918-62,940,330 SNORD27, SNORD22, 16 more genes
    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
    nsv5264892copy number variation1nstd204human GRCh38.p13 chr11: 62,843,236-62,855,465 , GRCh37.p13 chr11: 62,610,708-62,622,937 SLC3A2, SNORD26, 8 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
    nsv4492092mobile element insertion1nstd166human GRCh37.p13 chr11: 62,622,872-62,622,872 , GRCh38.p12 chr11: 62,855,400-62,855,400 SLC3A2, SNORD27, 3 more genes
    nsv4456974copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,487,052-62,788,240 , GRCh38.p12 chr11: 62,719,580-63,020,768 RN7SL259P, SNORD29, 29 more genes
    nsv4455787copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,314,663-62,788,240 , GRCh38.p12 chr11: 62,547,191-63,020,768 TTC9C, POLR2G, 48 more genes
    nsv4205678copy number variation1nstd166human GRCh37.p13 chr11: 62,622,535-62,622,726 , GRCh38.p12 chr11: 62,855,063-62,855,254 SLC3A2, SNORD28, 4 more genes
    nsv3922416copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,433,886-63,096,003 , NCBI36 chr11: 61,957,934-62,620,051 , GRCh37 chr11: 62,201,358-62,863,475 TAF6L, TMEM179B, 51 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