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Items: 1 to 20 of 127

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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
    nsv7072817inversion1nstd229human GRCh38 chr11: 62,534,346-62,603,459 , GRCh37.p13 chr11: 62,301,818-62,370,931 MTA2, MIR6747, 4 more genes
    nsv7071090inversion1nstd229human GRCh38 chr11: 62,568,277-62,606,017 , GRCh37.p13 chr11: 62,335,749-62,373,489 TUT1, EML3, 2 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
    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
    nsv6903418copy number variation1nstd229human GRCh38 chr11: 62,563,058-62,565,021 , GRCh37.p13 chr11: 62,330,530-62,332,493 EEF1G, MIR6747
    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
    nsv6462780copy number variation1nstd223human GRCh38 chr11: 62,563,058-62,565,021 , GRCh37.p13 chr11: 62,330,530-62,332,493 MIR6747, EEF1G
    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
    nsv6021309copy number variation1nstd212human GRCh38 chr11: 62,563,067-62,564,421 , GRCh37.p13 chr11: 62,330,539-62,331,893 EEF1G
    nsv5908826copy number variation1nstd209human GRCh38 chr11: 62,558,381-62,558,557 , GRCh37.p13 chr11: 62,325,853-62,326,029 EEF1G
    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
    nsv5268498copy number variation1nstd204human GRCh38.p13 chr11: 62,450,801-62,721,600 , GRCh37.p13 chr11: 62,218,273-62,489,072 HNRNPUL2-BSCL2, GANAB, 19 more genes
    nsv4979702copy number variation1nstd200human GRCh38 chr11: 62,563,057-62,565,026 , GRCh37.p13 chr11: 62,330,529-62,332,498 MIR6747, EEF1G
    nsv4839544copy number variation1nstd200human GRCh37 chr11: 62,330,530-62,332,498 , GRCh38.p12 chr11: 62,563,058-62,565,026 MIR6747, EEF1G
    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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
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