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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093757copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,103,138-121,060,609 , GRCh38.p12 chr11: 119,232,428-121,189,900 USP2-AS1, LOC101929208, 41 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7074550inversion1nstd229human GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063 VPS11, LOC100131626, 55 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6916257copy number variation1nstd229human GRCh38 chr11: 119,331,906-119,338,694 , GRCh37.p13 chr11: 119,202,616-119,209,404 RNF26, C1QTNF5, 1 more genes
    nsv6914602copy number variation1nstd229human GRCh38 chr11: 119,292,683-119,545,665 , GRCh37.p13 chr11: 119,163,393-119,416,375 MIR6756, RNF26, 9 more genes
    nsv6913229copy number variation1nstd229human GRCh38 chr11: 119,327,657-119,334,097 , GRCh37.p13 chr11: 119,198,367-119,204,807 RNF26
    nsv6464746copy number variation1nstd223human GRCh38 chr11: 119,333,685-119,352,569 , GRCh37.p13 chr11: 119,204,395-119,223,279 RNF26, C1QTNF5, 1 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
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv5657405insertion1nstd207human GRCh38 chr11: 119,332,675-119,332,675 , GRCh37.p13 chr11: 119,203,385-119,203,385 RNF26
    nsv5380954copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,077,108-120,133,495 , GRCh38.p12 chr11: 119,206,398-120,262,786 NECTIN1-DT, RNU6-262P, 29 more genes
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4600946copy number variation1nstd183human GRCh37 chr11: 119,207,104-119,207,148 , GRCh38.p12 chr11: 119,336,394-119,336,438 RNF26
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
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