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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094186copy number variation1nstd102humanUncertain significance GRCh37 chr11: 721,044-3,988,932 , GRCh38.p12 chr11: 721,044-3,967,702 OR7E117P, RPLP2, 124 more genes
    nsv7093761copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,278,740-2,906,719 , GRCh38.p12 chr11: 1,257,510-2,885,489 TOLLIP-DT, KRTAP5-6, 58 more genes
    nsv7063334inversion1nstd229human GRCh38 chr11: 1,656,321-1,685,165 , GRCh37.p13 chr11: 1,677,551-1,706,395 FAM99B, FAM99A
    nsv6888109copy number variation1nstd229human GRCh38 chr11: 1,558,735-1,701,768 , GRCh37.p13 chr11: 1,579,965-1,722,998 KRTAP5-4, FAM99A, 9 more genes
    nsv6885276copy number variation1nstd229human GRCh38 chr11: 1,136,035-3,145,463 , GRCh37.p13 chr11: 1,129,943-3,166,693 KRTAP5-1, MIR675, 69 more genes
    nsv6879718copy number variation1nstd229human GRCh38 chr11: 1,203,314-1,714,253 , GRCh37.p13 chr11: 1,224,544-1,735,483 KRTAP5-3, KRTAP5-2, 17 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6620713copy number variation1nstd224human GRCh37 chr11: 1,629,693-1,881,256 , GRCh38.p12 chr11: 1,608,463-1,860,026 , GRCh38.p12 chr11|NT_187657.1: 85,016-214,625 TNNI2, KRTAP5-3, 15 more genes
    nsv6594407inversion1nstd223human GRCh38 chr11: 1,667,189-1,683,495 , GRCh37.p13 chr11: 1,688,419-1,704,725 FAM99B, FAM99A
    nsv6588417inversion1nstd223human GRCh38 chr11: 1,667,405-1,683,364 , GRCh37.p13 chr11: 1,688,635-1,704,594 FAM99B, FAM99A
    nsv6438165copy number variation1nstd223human GRCh38 chr11: 737,066-3,896,161 , GRCh37.p13 chr11: 737,066-3,917,391 RNU6-878P, CARS1-AS1, 123 more genes
    nsv6315550copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,621,232-2,228,572 , GRCh38.p12 chr11: 1,600,002-2,207,342 IGF2-AS, SNORD131, 31 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6281400insertion1nstd214human GRCh38 chr11: 1,666,179-1,666,179 , GRCh37.p13 chr11: 1,687,409-1,687,409 FAM99A
    nsv6279373insertion1nstd214human GRCh38 chr11: 1,666,264-1,666,264 , GRCh37.p13 chr11: 1,687,494-1,687,494 FAM99A
    nsv6278539insertion2nstd214human GRCh38 chr11: 1,665,596-1,665,596 , GRCh37.p13 chr11: 1,686,826-1,686,826 FAM99A
    nsv6144033copy number variation1nstd206human GRCh38 chr11: 1,661,000-1,666,300 , GRCh37.p13 chr11: 1,682,230-1,687,530 FAM99A
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