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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
    nsv7069463inversion1nstd229human GRCh38 chr11: 64,441,902-64,755,854 , GRCh37.p13 chr11: 64,209,374-64,523,326 NRXN2, SLC22A12, 5 more genes
    nsv7061071inversion1nstd229human GRCh38 chr11: 64,416,765-64,622,794 , GRCh37.p13 chr11: 64,184,237-64,390,266 NRXN2, SLC22A11, 3 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
    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
    nsv6898936copy number variation1nstd229human GRCh38 chr11: 64,444,801-64,452,900 , GRCh37.p13 chr11: 64,212,273-64,220,372 LINC02724
    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
    nsv6132184copy number variation1nstd213human GRCh37 chr11: 64,210,000-64,390,001 , GRCh38.p12 chr11: 64,442,528-64,622,529 NRXN2, SLC22A11, 2 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
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 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
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv2784395copy number variation1nstd132human NCBI36 chr11: 63,563,569-63,980,103 , GRCh37.p13 chr11: 63,806,993-64,223,527 , GRCh38.p12 chr11: 64,039,521-64,456,055 ESRRA, DNAJC4, 28 more genes
    nsv1589977short tandem repeat2nstd128human GRCh37 chr11: 64,214,716-64,214,747 , GRCh38.p12 chr11: 64,447,244-64,447,275 LINC02724
    nsv1589267short tandem repeat6nstd128human GRCh37 chr11: 64,218,521-64,218,534 , GRCh38.p12 chr11: 64,451,049-64,451,062 LINC02724
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