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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5139339mobile element insertion1nstd203human GRCh38 chr11: 63,913,491-63,913,500 , GRCh37.p13 chr11: 63,680,963-63,680,972 RCOR2
    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
    nsv4668493copy number variation1nstd186human GRCh37 chr11: 63,676,301-63,685,500 , GRCh38.p12 chr11: 63,908,829-63,918,028 MARK2, RCOR2
    nsv4608492copy number variation1nstd183human GRCh37 chr11: 63,676,301-63,685,500 , GRCh38.p12 chr11: 63,908,829-63,918,028 MARK2, RCOR2
    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
    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
    nsv3909158copy number variation1nstd102humanBenign GRCh37 chr11: 63,594,517-63,680,369 , GRCh38.p12 chr11: 63,827,045-63,912,897 MARK2, ATP5MGP1, 4 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
    nsv3150079copy number variation1nstd151human GRCh37 chr11: 63,663,049-63,721,956 , GRCh38.p12 chr11: 63,895,577-63,954,484 RCOR2, NAA40, 1 more genes
    nsv3148594copy number variation1nstd151human GRCh37 chr11: 62,910,848-63,765,023 , GRCh38.p12 chr11: 63,143,376-63,997,551 , SLC22A10, 29 more genes
    nsv3140049copy number variation1nstd151human GRCh37 chr11: 63,681,886-63,682,431 , GRCh38.p12 chr11: 63,914,414-63,914,959 RCOR2
    nsv2787281copy number variation1nstd132human NCBI36 chr11: 63,420,882-63,586,382 , GRCh37.p13 chr11: 63,664,306-63,829,806 , GRCh38.p12 chr11: 63,896,834-64,062,334 , COX8A, 7 more genes
    nsv2784057copy number variation1nstd132human NCBI36 chr11: 63,435,368-63,688,067 , GRCh37.p13 chr11: 63,678,792-63,931,491 , GRCh38.p12 chr11: 63,911,320-64,164,019 , COX8A, 7 more genes
    nsv2783584copy number variation1nstd132human NCBI36 chr11: 63,435,368-63,595,613 , GRCh37.p13 chr11: 63,678,792-63,839,037 , GRCh38.p12 chr11: 63,911,320-64,071,565 , COX8A, 7 more genes
    nsv2783507copy number variation1nstd132human NCBI36 chr11: 63,435,368-63,666,729 , GRCh37.p13 chr11: 63,678,792-63,910,153 , GRCh38.p12 chr11: 63,911,320-64,142,681 , COX8A, 7 more genes
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