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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
    nsv6917523copy number variation1nstd229human GRCh38 chr11: 62,683,914-62,684,661 , GRCh37.p13 chr11: 62,451,386-62,452,133 LRRN4CL
    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
    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
    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
    nsv6309225copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,380,754-62,472,984 , GRCh38.p12 chr11: 62,613,282-62,705,512 GANAB, HNRNPUL2-BSCL2, 12 more genes
    nsv6248127mobile element insertion1nstd215human GRCh38 chr11: 62,686,539-62,686,539 , GRCh37.p13 chr11: 62,454,011-62,454,011 LRRN4CL
    nsv5909011copy number variation1nstd209human GRCh38 chr11: 62,687,086-62,688,239 , GRCh37.p13 chr11: 62,454,558-62,455,711 LRRN4CL
    nsv5699278mobile element insertion1nstd211human GRCh38 chr11: 62,686,501-62,686,501 , GRCh37.p13 chr11: 62,453,973-62,453,973 LRRN4CL
    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
    nsv5268235copy number variation1nstd204human GRCh38.p13 chr11: 62,664,401-62,843,200 , GRCh37.p13 chr11: 62,431,873-62,610,672 HNRNPUL2, UQCC3, 23 more genes
    nsv4979706copy number variation1nstd200human GRCh38 chr11: 62,683,976-62,684,596 , GRCh37.p13 chr11: 62,451,448-62,452,068 LRRN4CL
    nsv4849398copy number variation1nstd200human GRCh37 chr11: 62,454,559-62,455,715 , GRCh38.p12 chr11: 62,687,087-62,688,243 LRRN4CL
    nsv4846180copy number variation1nstd200human GRCh37 chr11: 62,451,448-62,452,068 , GRCh38.p12 chr11: 62,683,976-62,684,596 LRRN4CL
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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