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Items: 1 to 20 of 103

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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
    nsv7072675inversion1nstd229human GRCh38 chr11: 60,917,917-61,141,300 , GRCh37.p13 chr11: 60,685,389-60,908,772 SLC15A3, LOC105369325, 8 more genes
    nsv7070192inversion1nstd229human GRCh38 chr11: 60,947,732-60,950,000 , GRCh37.p13 chr11: 60,715,204-60,717,472 SLC15A3
    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
    nsv6912169copy number variation1nstd229human GRCh38 chr11: 60,931,371-60,964,610 , GRCh37.p13 chr11: 60,698,843-60,732,082 SLC15A3, TMEM132A
    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
    nsv6904848copy number variation1nstd229human GRCh38 chr11: 60,943,401-60,946,700 , GRCh37.p13 chr11: 60,710,873-60,714,172 SLC15A3
    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
    nsv6898161copy number variation1nstd229human GRCh38 chr11: 60,940,814-60,947,607 , GRCh37.p13 chr11: 60,708,286-60,715,079 SLC15A3
    nsv6472998copy number variation1nstd223human GRCh38 chr11: 60,943,394-60,946,685 , GRCh37.p13 chr11: 60,710,866-60,714,157 SLC15A3
    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
    nsv5701958mobile element insertion1nstd211human GRCh38 chr11: 60,949,571-60,949,571 , GRCh37.p13 chr11: 60,717,043-60,717,043 SLC15A3
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984990copy number variation1nstd200human GRCh38 chr11: 60,931,698-60,971,997 , GRCh37.p13 chr11: 60,699,170-60,739,469 SLC15A3, CD6, 1 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 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
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