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    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
    nsv6914219copy number variation1nstd229human GRCh38 chr11: 62,836,654-62,850,116 , GRCh37.p13 chr11: 62,604,126-62,617,588 RNU2-2P, WDR74, 1 more genes
    nsv6910321copy number variation1nstd229human GRCh38 chr11: 62,841,577-62,841,622 , GRCh37.p13 chr11: 62,609,049-62,609,094 WDR74, RNU2-2P
    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
    nsv6904195copy number variation1nstd229human GRCh38 chr11: 62,841,189-62,841,245 , GRCh37.p13 chr11: 62,608,661-62,608,717 RNU2-2P, WDR74
    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
    nsv6586429inversion1nstd223human GRCh38 chr11: 62,837,675-62,850,312 , GRCh37.p13 chr11: 62,605,147-62,617,784 SNHG1, RNU2-2P, 1 more genes
    nsv6464851copy number variation1nstd223human GRCh38 chr11: 62,831,466-62,852,682 , GRCh37.p13 chr11: 62,598,938-62,620,154 STX5, WDR74, 8 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
    nsv6248129mobile element insertion1nstd215human GRCh38 chr11: 62,836,146-62,836,146 , GRCh37.p13 chr11: 62,603,618-62,603,618 WDR74
    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
    nsv5373663translocation1nstd200human GRCh38 chr11: 62,847,118-62,847,118 , GRCh38 chr11: 62,838,160-62,838,160 , GRCh37.p13 chr11: 62,614,590-62,614,590 , GRCh37.p13 chr11: 62,605,632-62,605,632 WDR74
    nsv5373662translocation1nstd200human GRCh38 chr11: 62,850,312-62,850,312 , GRCh38 chr11: 62,837,675-62,837,675 , GRCh37.p13 chr11: 62,605,147-62,605,147 , GRCh37.p13 chr11: 62,617,784-62,617,784 SNHG1, WDR74
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