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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923551copy number variation1nstd209human GRCh38 chr11: 20,096,010-20,731,492 , GRCh37.p13 chr11: 20,117,556-20,753,038 , HMGB1P40, 9 more genes
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5505604copy number variation1nstd206human GRCh38 chr11: 20,372,111-20,372,194 , GRCh37.p13 chr11: 20,393,657-20,393,740 HTATIP2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5345624translocation1nstd200human GRCh37 chr11: 20,393,657-20,393,657 , GRCh37 chr11: 20,393,740-20,393,740 , GRCh38.p12 chr11: 20,372,111-20,372,111 , GRCh38.p12 chr11: 20,372,194-20,372,194 HTATIP2
    nsv4984252copy number variation1nstd200human GRCh38 chr11: 20,159,358-20,476,084 , GRCh37.p13 chr11: 20,180,904-20,497,630 LOC105376583, DBX1, 2 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
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 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
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4201794copy number variation1nstd166human GRCh37.p13 chr11: 20,393,657-20,393,740 , GRCh38.p12 chr11: 20,372,111-20,372,194 HTATIP2
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3921634copy number variation1nstd102humanUncertain significance NCBI36 chr11: 18,504,345-20,726,247 , GRCh38 chr11: 18,526,222-20,748,125 , GRCh37 chr11: 18,547,769-20,769,671 NELL1, UEVLD, 41 more genes
    nsv3916031copy number variation1nstd102humanUncertain significance GRCh38 chr11: 20,375,594-20,634,327 , NCBI36 chr11: 20,353,716-20,612,449 , GRCh37 chr11: 20,397,140-20,655,873 LOC105376584, SLC6A5, 3 more genes
    nsv3910826copy number variation1nstd102humanUncertain significance NCBI36 chr11: 20,287,388-20,976,611 , GRCh37.p13 chr11: 20,330,812-21,020,035 , GRCh38.p12 chr11: 20,309,266-20,998,489 PRMT3, LOC105376584, 5 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
    nsv3901577copy number variation1nstd102humanPathogenic GRCh37 chr11: 18,536,224-31,923,308 , GRCh38.p12 chr11: 18,514,677-31,901,762 LOC105376588, LOC105376585, 137 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
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