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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093918copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641 PAFAH1B2, FXYD2, 26 more genes
    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
    nsv6908236copy number variation1nstd229human GRCh38 chr11: 116,806,714-116,840,427 , GRCh37.p13 chr11: 116,677,430-116,711,143 APOA4, APOA1-AS, 2 more genes
    nsv6907901copy number variation1nstd229human GRCh38 chr11: 116,801,301-116,830,600 , GRCh37.p13 chr11: 116,672,017-116,701,316 APOA4, APOC3
    nsv6637620copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,464-116,711,974 , GRCh38.p12 chr11: 116,789,748-116,841,258 APOA1, ZPR1, 4 more genes
    nsv6636022copy number variation1nstd102humanPathogenic GRCh38 chr11: 116,800,700-116,841,000 , GRCh37.p13 chr11: 116,671,416-116,711,716 APOA1, APOC3, 2 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 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
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 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
    nsv6132077copy number variation1nstd213human GRCh37 chr11: 116,320,000-116,730,001 , GRCh38.p12 chr11: 116,449,283-116,859,285 APOA4, LOC107984372, 9 more genes
    nsv5512453copy number variation1nstd206human GRCh38 chr11: 116,832,660-116,832,926 , GRCh37.p13 chr11: 116,703,376-116,703,642 APOC3
    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
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4980858copy number variation1nstd200human GRCh38 chr11: 116,832,469-116,832,575 , GRCh37.p13 chr11: 116,703,185-116,703,291 APOC3
    nsv4980857copy number variation1nstd200human GRCh38 chr11: 116,823,523-116,830,641 , GRCh37.p13 chr11: 116,694,239-116,701,357 APOC3, APOA4
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 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
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