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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699620mobile element insertion2nstd211human GRCh38 chr11: 6,602,361-6,602,361 , GRCh37.p13 chr11: 6,623,591-6,623,591 ILK, RRP8
    nsv5672634copy number variation1nstd102humanPathogenic GRCh37 chr11: 6,559,613-6,640,631 , GRCh38.p12 chr11: 6,538,383-6,619,400 TPP1, ILK, 4 more genes
    nsv4978067copy number variation1nstd200human GRCh38 chr11: 6,595,776-6,605,206 , GRCh37.p13 chr11: 6,617,006-6,626,436 ILK, RRP8, 1 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
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 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
    nsv4615667copy number variation1nstd183human GRCh37 chr11: 6,629,883-6,629,928 , GRCh38.p12 chr11: 6,608,653-6,608,698 ILK, TAF10
    nsv4605947copy number variation1nstd183human GRCh37 chr11: 6,616,815-6,629,336 , GRCh38.p12 chr11: 6,595,585-6,608,106 TAF10, ILK, 1 more genes
    nsv4552213insertion1nstd166human GRCh37.p13 chr11: 6,623,573-6,623,573 , GRCh38.p12 chr11: 6,602,343-6,602,343 RRP8, ILK
    nsv4456790copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,607,967-6,796,286 , GRCh38.p12 chr11: 6,586,737-6,775,055 ILK, MRPL17, 8 more genes
    nsv4456235copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621 OR52X1P, LOC112268071, 40 more genes
    nsv4370152copy number variation1nstd173human GRCh37 chr11: 6,629,042-8,085,652 , GRCh38.p12 chr11: 6,607,812-8,064,105 LOC105376533, GVINP2, 48 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
    nsv3956686copy number variation1nstd168human GRCh38 chr11: 6,597,192-6,616,322 , GRCh37.p13 chr11: 6,618,422-6,637,553 RRP8, TPP1, 2 more genes
    nsv3955996insertion1nstd168human GRCh38 chr11: 6,606,266-6,611,025 , GRCh37.p13 chr11: 6,627,496-6,632,256 TPP1, ILK, 1 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3915725copy number variation1nstd102humanPathogenic NCBI36 chr11: 6,239,388-6,615,806 , GRCh38 chr11: 6,261,582-6,637,999 , GRCh37 chr11: 6,282,812-6,659,230 TRIM3, LOC101927825, 14 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
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