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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5249964copy number variation1nstd204human GRCh38.p13 chr11: 6,454,117-6,456,591 , GRCh37.p13 chr11: 6,475,347-6,477,821 TRIM3
    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
    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
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4210864copy number variation1nstd166human GRCh37.p13 chr11: 6,442,783-6,486,112 , GRCh38.p12 chr11: 6,421,553-6,464,882 TRIM3, HPX
    nsv4200885copy number variation1nstd166human GRCh37.p13 chr11: 6,495,000-6,504,000 , GRCh38.p12 chr11: 6,473,770-6,482,770 ARFIP2, TIMM10B, 1 more genes
    nsv4193150copy number variation1nstd166human GRCh37.p13 chr11: 6,492,364-6,492,429 , GRCh38.p12 chr11: 6,471,134-6,471,199 TRIM3
    nsv4192612copy number variation1nstd166human GRCh37.p13 chr11: 6,469,119-6,469,626 , GRCh38.p12 chr11: 6,447,889-6,448,396 TRIM3
    nsv3971474insertion1nstd168human GRCh38 chr11: 6,450,124-6,452,615 , GRCh37.p13 chr11: 6,471,354-6,473,845 TRIM3
    nsv3958240copy number variation1nstd168human GRCh38 chr11: 6,439,798-6,450,124 , GRCh37.p13 chr11: 6,461,028-6,471,354 TRIM3, HPX
    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
    nsv3912381copy number variation1nstd102humanUncertain significance NCBI36 chr11: 5,571,015-6,424,808 , GRCh37 chr11: 5,614,439-6,468,232 , GRCh38 chr11: 5,593,209-6,447,002 OR52E6, TRIM34, 46 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
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