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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
    nsv7075313inversion1nstd229human GRCh38 chr11: 62,887,478-63,793,002 , GRCh37.p13 chr11: 62,654,950-63,560,474 RPL29P22, TUBAP7, 25 more genes
    nsv7060800inversion1nstd229human GRCh38 chr11: 62,887,439-63,792,997 , GRCh37.p13 chr11: 62,654,911-63,560,469 TUBAP7, ATL3, 25 more genes
    nsv7058098inversion1nstd229human GRCh38 chr11: 62,887,432-63,795,073 , GRCh37.p13 chr11: 62,654,904-63,562,545 TUBAP7, ATL3, 25 more genes
    nsv6909374copy number variation1nstd229human GRCh38 chr11: 63,513,117-63,513,575 , GRCh37.p13 chr11: 63,280,589-63,281,047 LGALS12
    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
    nsv6621194copy number variation1nstd224human GRCh37 chr11: 63,064,887-63,350,253 , GRCh38.p12 chr11: 63,297,415-63,582,781 PLAAT2, SLC22A10, 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
    nsv6132371copy number variation1nstd213human GRCh37 chr11: 63,120,000-64,210,001 , GRCh38.p12 chr11: 63,352,528-64,442,529 VEGFB, FLRT1, 51 more genes
    nsv6132183copy number variation1nstd213human GRCh37 chr11: 63,160,000-63,380,001 , GRCh38.p12 chr11: 63,392,528-63,612,529 PLAAT4, TMSB4XP5, 7 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
    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
    nsv4729316copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,714,816-63,383,226 , GRCh38.p12 chr11: 62,947,344-63,615,754 LOC105369334, PLAAT3, 18 more genes
    nsv3969050insertion1nstd168human GRCh38 chr11: 63,393,307-63,506,568 , GRCh37.p13 chr11: 63,160,779-63,274,040 LGALS12, SLC22A9, 2 more genes
    nsv3959811copy number variation1nstd168human GRCh38 chr11: 63,401,070-63,536,204 , GRCh37.p13 chr11: 63,168,542-63,303,676 PLAAT4, TMSB4XP5, 4 more genes
    nsv3924003copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 62,417,274-63,859,091 , GRCh37 chr11: 62,660,698-64,102,515 , GRCh38 chr11: 62,893,226-64,335,043 BAD, CCND2P1, 58 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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