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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5253953copy number variation1nstd204human GRCh38.p13 chr11: 2,400,895-2,403,494 , GRCh37.p13 chr11: 2,422,125-2,424,724 TSSC4, TRPM5
    nsv5253123copy number variation1nstd204human GRCh38.p13 chr11: 2,398,295-2,401,594 , GRCh37.p13 chr11: 2,419,525-2,422,824 TSSC4
    nsv4977882copy number variation1nstd200human GRCh38 chr11: 2,399,240-2,399,343 , GRCh37.p13 chr11: 2,420,470-2,420,573 TSSC4
    nsv4843317copy number variation1nstd200human GRCh37 chr11: 2,420,470-2,420,573 , GRCh38.p12 chr11: 2,399,240-2,399,343 TSSC4
    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
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4728784copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,316,896-2,418,571 , GRCh38.p12 chr11: 2,295,666-2,397,341 LOC105376520, CD81, 6 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 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
    nsv4675807copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,209,396-2,520,511 , GRCh38.p12 chr11: 2,188,166-2,499,281 ASCL2, CD81, 9 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
    nsv4415109copy number variation1nstd174human GRCh37 chr11: 2,396,201-2,418,430 , GRCh38.p12 chr11: 2,374,971-2,397,200 CD81-AS1, CD81, 2 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4207291copy number variation1nstd166human GRCh37.p13 chr11: 2,421,317-2,421,368 , GRCh38.p12 chr11: 2,400,087-2,400,138 TSSC4
    nsv4196666copy number variation1nstd166human GRCh37.p13 chr11: 2,420,470-2,420,573 , GRCh38.p12 chr11: 2,399,240-2,399,343 TSSC4
    nsv3924864copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,996,741-3,645,369 , NCBI36 chr11: 1,953,317-3,601,945 , GRCh38 chr11: 1,975,511-3,624,139 TSSC2, CD81, 54 more genes
    nsv3922910copy number variation1nstd102humanPathogenic NCBI36 chr11: 1,116,807-3,191,729 , GRCh38 chr11: 1,132,899-3,213,923 , GRCh37 chr11: 1,126,807-3,235,153 CARS1-AS1, TH, 69 more genes
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