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Items: 1 to 20 of 268

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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
    nsv5649341insertion1nstd207human GRCh38 chr11: 2,422,013-2,422,013 , GRCh37.p13 chr11: 2,443,243-2,443,243 TRPM5
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5316036copy number variation1nstd204human GRCh38.p13 chr11: 2,411,609-2,411,859 , GRCh37.p13 chr11: 2,432,839-2,433,089 TRPM5
    nsv5259246copy number variation1nstd204human GRCh38.p13 chr11: 2,411,495-2,412,613 , GRCh37.p13 chr11: 2,432,725-2,433,843 TRPM5
    nsv5253953copy number variation1nstd204human GRCh38.p13 chr11: 2,400,895-2,403,494 , GRCh37.p13 chr11: 2,422,125-2,424,724 TSSC4, TRPM5
    nsv4977883copy number variation1nstd200human GRCh38 chr11: 2,406,456-2,411,857 , GRCh37.p13 chr11: 2,427,686-2,433,087 TRPM5
    nsv4842211copy number variation1nstd200human GRCh37 chr11: 2,430,013-2,430,377 , GRCh38.p12 chr11: 2,408,783-2,409,147 TRPM5
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4754833insertion1nstd199human GRCh37 chr11: 2,443,215-2,443,215 , GRCh38.p12 chr11: 2,421,985-2,421,985 TRPM5
    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
    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
    nsv4607262copy number variation1nstd183human GRCh37 chr11: 2,439,638-2,441,010 , GRCh38.p12 chr11: 2,418,408-2,419,780 TRPM5
    nsv4604218copy number variation1nstd183human GRCh37 chr11: 2,439,753-2,439,907 , GRCh38.p12 chr11: 2,418,523-2,418,677 TRPM5
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4206467copy number variation1nstd166human GRCh37.p13 chr11: 2,425,616-2,428,557 , GRCh38.p12 chr11: 2,404,386-2,407,327 TRPM5
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