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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094286copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,987,528-41,230,232 , GRCh38.p12 chr15: 40,695,330-40,938,034 PPP1R14D, LOC105370943, 13 more genes
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv7059477inversion1nstd229human GRCh38 chr15: 40,700,806-40,921,327 , GRCh37.p13 chr15: 40,993,004-41,213,525 RAD51, SUMO2P15, 11 more genes
    nsv7059363inversion1nstd229human GRCh38 chr15: 40,487,055-41,342,774 , GRCh37.p13 chr15: 40,779,254-41,634,972 DLL4, CHP1, 33 more genes
    nsv7058611inversion1nstd229human GRCh38 chr15: 40,677,443-40,883,578 , GRCh37.p13 chr15: 40,969,641-41,175,776 SPINT1-AS1, DNAJC17, 10 more genes
    nsv6967230copy number variation1nstd229human GRCh38 chr15: 40,677,546-40,812,141 , GRCh37.p13 chr15: 40,969,744-41,104,339 RAD51-AS1, C15orf62, 6 more genes
    nsv6966448copy number variation1nstd229human GRCh38 chr15: 40,764,501-40,912,500 , GRCh37.p13 chr15: 41,056,699-41,204,698 ZFYVE19, DNAJC17, 8 more genes
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729095copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,464,942-41,196,807 , GRCh38.p12 chr15: 40,172,741-40,904,609 SPINT1-AS1, KNSTRN, 37 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4235888copy number variation1nstd166human GRCh37.p13 chr15: 41,049,000-41,073,500 , GRCh38.p12 chr15: 40,756,802-40,781,302 GCHFR, DNAJC17, 2 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
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