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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
    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
    nsv4608392copy number variation1nstd183human GRCh37 chr11: 63,535,644-63,536,914 , GRCh38.p12 chr11: 63,768,172-63,769,442 ZFTA
    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
    nsv4212286copy number variation1nstd166human GRCh37.p13 chr11: 63,530,775-63,530,836 , GRCh38.p12 chr11: 63,763,303-63,763,364 ZFTA
    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
    nsv3907873copy number variation1nstd102humanBenign GRCh37 chr11: 63,410,966-63,525,778 , GRCh38.p12 chr11: 63,643,494-63,758,306 ATL3, ZFTA, 1 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
    nsv3148594copy number variation1nstd151human GRCh37 chr11: 62,910,848-63,765,023 , GRCh38.p12 chr11: 63,143,376-63,997,551 , SLC22A10, 29 more genes
    nsv1590492short tandem repeat3nstd128human GRCh37 chr11: 63,531,514-63,531,555 , GRCh38.p12 chr11: 63,764,042-63,764,083 ZFTA
    nsv1590491short tandem repeat5nstd128human GRCh37 chr11: 63,527,192-63,527,206 , GRCh38.p12 chr11: 63,759,720-63,759,734 RTN3, ZFTA
    nsv1588452short tandem repeat3nstd128human GRCh37 chr11: 63,533,315-63,533,354 , GRCh38.p12 chr11: 63,765,843-63,765,882 ZFTA
    nsv1588451short tandem repeat2nstd128human GRCh37 chr11: 63,531,210-63,531,246 , GRCh38.p12 chr11: 63,763,738-63,763,774 ZFTA
    nsv1588450short tandem repeat2nstd128human GRCh37 chr11: 63,530,461-63,530,482 , GRCh38.p12 chr11: 63,762,989-63,763,010 ZFTA
    nsv1588449short tandem repeat7nstd128human GRCh37 chr11: 63,527,341-63,527,354 , GRCh38.p12 chr11: 63,759,869-63,759,882 RTN3, ZFTA
    nsv1587347short tandem repeat1nstd128human GRCh37 chr11: 63,531,906-63,531,930 , GRCh38.p12 chr11: 63,764,434-63,764,458 ZFTA
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