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Items: 1 to 20 of 125

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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
    nsv7093756copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,967,708-119,103,425 , GRCh38.p12 chr11: 119,096,998-119,232,715 CBL, HINFP, 7 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
    nsv7066555inversion1nstd229human GRCh38 chr11: 119,191,746-119,196,417 , GRCh37.p13 chr11: 119,062,455-119,067,127 CCDC153
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6902025copy number variation1nstd229human GRCh38 chr11: 118,757,701-119,235,300 , GRCh37.p13 chr11: 118,635,052-119,106,010 UPK2, VPS11, 25 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
    nsv6291385copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,849,155-119,067,781 , GRCh38.p12 chr11: 118,978,445-119,197,071 RPS25, C2CD2L, 17 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
    nsv5497641copy number variation1nstd206human GRCh38 chr11: 119,191,758-119,205,489 , GRCh37.p13 chr11: 119,062,467-119,076,199 CCDC153, CBL
    nsv5130140mobile element insertion1nstd203human GRCh38 chr11: 119,191,312-119,191,327 , GRCh37.p13 chr11: 119,062,021-119,062,036 CCDC153
    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
    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
    nsv4451218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801 ABCG4, CCDC153, 52 more genes
    nsv4450648copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 118,967,698-119,170,501 , GRCh38.p12 chr11: 119,096,988-119,299,791 NLRX1, SNORD150, 8 more genes
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