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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4978005copy number variation1nstd200human GRCh38 chr11: 5,351,084-5,363,532 , GRCh37.p13 chr11: 5,372,314-5,384,762 TMEM258P1, LOC100418885, 2 more genes
    nsv4978004copy number variation1nstd200human GRCh38 chr11: 5,350,419-5,351,857 , GRCh37.p13 chr11: 5,371,649-5,373,087 OR51B5, OR51B6
    nsv4978002copy number variation1nstd200human GRCh38 chr11: 5,339,877-5,351,114 , GRCh37.p13 chr11: 5,361,107-5,372,344 OR51B6, OR51B5
    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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4617597copy number variation1nstd183human GRCh37 chr11: 5,372,517-5,384,714 , GRCh38.p12 chr11: 5,351,287-5,363,484 LOC100418885, TMEM258P1, 2 more genes
    nsv4612348copy number variation1nstd183human GRCh37 chr11: 5,328,528-5,642,684 , GRCh38.p12 chr11: 5,307,298-5,621,454 OR51B3P, OR51I2, 27 more genes
    nsv4599589copy number variation1nstd183human GRCh37 chr11: 5,367,298-5,384,223 , GRCh38.p12 chr11: 5,346,068-5,362,993 TMEM258P1, LOC100418885, 2 more genes
    nsv4387795copy number variation1nstd173human GRCh37 chr11: 5,067,391-6,257,231 , GRCh38.p12 chr11: 5,046,161-6,236,001 HBD, OR52N2, 85 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
    nsv4345375sequence alteration1nstd166human GRCh37.p13 chr11: 5,037,622-5,455,788 , GRCh38.p12 chr11: 5,016,392-5,434,558 HBB, HBE1, 32 more genes
    nsv4193819copy number variation1nstd166human GRCh37.p13 chr11: 5,371,649-5,373,087 , GRCh38.p12 chr11: 5,350,419-5,351,857 OR51B5, OR51B6
    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
    nsv3918376copy number variation1nstd102humanPathogenic NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927 HBG2, OR51T1, 262 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
    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
    nsv3900835copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,361,271-5,616,544 , GRCh38.p12 chr11: 5,340,041-5,595,314 TRIM6-TRIM34, UBQLNL, 23 more genes
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