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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922220copy number variation1nstd209human GRCh38 chr11: 3,495,175-3,643,117 , GRCh37.p13 chr11: 3,516,405-3,664,347 ART1, XNDC1CP, 9 more genes
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5913860copy number variation1nstd209human GRCh38 chr11: 3,630,637-3,640,994 , GRCh37.p13 chr11: 3,651,867-3,662,224 TRPC2, ART5
    nsv5857367copy number variation2nstd209human GRCh38 chr11: 3,630,668-3,640,979 , GRCh37.p13 chr11: 3,651,898-3,662,209 ART5, TRPC2
    nsv5513578copy number variation1nstd206human GRCh38 chr11: 3,598,372-3,731,278 , GRCh37.p13 chr11: 3,619,602-3,752,508 ART1, NUP98, 6 more genes
    nsv5510086copy number variation1nstd206human GRCh38 chr11: 3,630,606-3,641,045 , GRCh37.p13 chr11: 3,651,836-3,662,275 ART5, TRPC2
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv4984148copy number variation1nstd200human GRCh38 chr11: 3,595,545-3,641,059 , GRCh37.p13 chr11: 3,616,775-3,662,289 TRPC2, OR7E117P, 2 more genes
    nsv4977929copy number variation1nstd200human GRCh38 chr11: 3,640,622-3,640,767 , GRCh37.p13 chr11: 3,661,852-3,661,997 ART5
    nsv4977927copy number variation1nstd200human GRCh38 chr11: 3,613,666-3,650,797 , GRCh37.p13 chr11: 3,634,896-3,672,027 ART5, TRPC2, 2 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 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
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4679705copy number variation1nstd189human GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027 , ART1, 50 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4616868copy number variation1nstd183human GRCh37 chr11: 3,426,081-3,674,989 , GRCh38.p12 chr11: 3,404,851-3,653,759 , RPS24P14, 13 more genes
    nsv4616173copy number variation1nstd183human GRCh37 chr11: 3,651,867-3,662,225 , GRCh38.p12 chr11: 3,630,637-3,640,995 ART5, TRPC2
    nsv4605212copy number variation1nstd183human GRCh37 chr11: 3,647,274-3,904,364 , GRCh38.p12 chr11: 3,626,044-3,883,134 NUP98, RHOG, 10 more genes
    nsv4578642copy number variation1nstd102humanUncertain significance GRCh37 chr11: 3,659,968-3,746,449 , GRCh38.p12 chr11: 3,638,738-3,725,219 ART5, RNU6-1143P, 3 more genes
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