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Items: 1 to 20 of 153

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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
    nsv7077662inversion1nstd229human GRCh38 chr11: 61,141,297-61,168,693 , GRCh37.p13 chr11: 60,908,769-60,936,165 VPS37C
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7072675inversion1nstd229human GRCh38 chr11: 60,917,917-61,141,300 , GRCh37.p13 chr11: 60,685,389-60,908,772 SLC15A3, LOC105369325, 8 more genes
    nsv6916336copy number variation1nstd229human GRCh38 chr11: 61,141,401-61,159,000 , GRCh37.p13 chr11: 60,908,873-60,926,472 VPS37C
    nsv6914367copy number variation1nstd229human GRCh38 chr11: 61,157,035-61,158,886 , GRCh37.p13 chr11: 60,924,507-60,926,358 VPS37C
    nsv6914360copy number variation1nstd229human GRCh38 chr11: 61,137,796-61,138,154 , GRCh37.p13 chr11: 60,905,268-60,905,626 VPS37C
    nsv6913144copy number variation1nstd229human GRCh38 chr11: 60,917,901-61,168,700 , GRCh37.p13 chr11: 60,685,373-60,936,172 LOC105369325, TMEM109, 8 more genes
    nsv6907950copy number variation1nstd229human GRCh38 chr11: 61,129,857-61,130,467 , GRCh37.p13 chr11: 60,897,329-60,897,939 VPS37C
    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
    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
    nsv6461797copy number variation1nstd223human GRCh38 chr11: 61,131,627-61,132,386 , GRCh37.p13 chr11: 60,899,099-60,899,858 VPS37C
    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
    nsv6093491insertion1nstd212human GRCh38 chr11: 61,159,891-61,159,891 , GRCh37.p13 chr11: 60,927,363-60,927,363 VPS37C
    nsv5915970copy number variation1nstd209human GRCh38 chr11: 61,156,826-61,156,978 , GRCh37.p13 chr11: 60,924,298-60,924,450 VPS37C
    nsv5915582copy number variation1nstd209human GRCh38 chr11: 61,149,797-61,168,615 , GRCh37.p13 chr11: 60,917,269-60,936,087 VPS37C
    nsv5864245copy number variation1nstd209human GRCh38 chr11: 61,132,436-61,133,974 , GRCh37.p13 chr11: 60,899,908-60,901,446 VPS37C
    nsv5851238copy number variation1nstd209human GRCh38 chr11: 61,149,705-61,168,687 , GRCh37.p13 chr11: 60,917,177-60,936,159 VPS37C
    nsv5700597mobile element insertion2nstd211human GRCh38 chr11: 61,138,636-61,138,636 , GRCh37.p13 chr11: 60,906,108-60,906,108 VPS37C
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