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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120714copy number variation1nstd186human GRCh37 chr15: 25,458,462-25,458,605 , GRCh38.p12 chr15: 25,213,315-25,213,458 SNORD115-24, SNHG14
    nsv6112770copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,616,095-28,538,904 , GRCh38.p12 chr15: 23,370,948-28,293,758 LOC105370728, SNORD115-14, 144 more genes
    nsv5940717copy number variation1nstd209human GRCh38 chr15: 25,213,315-25,213,456 , GRCh37.p13 chr15: 25,458,462-25,458,603 SNORD115-24, SNHG14
    nsv5936547copy number variation1nstd209human GRCh38 chr15: 25,213,044-25,214,381 , GRCh37.p13 chr15: 25,458,191-25,459,528 SNORD115-25, SNORD115-24, 1 more genes
    nsv5864698copy number variation1nstd209human GRCh38 chr15: 25,213,068-25,214,367 , GRCh37.p13 chr15: 25,458,215-25,459,514 SNORD115-24, SNORD115-25, 1 more genes
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5596542copy number variation1nstd207human GRCh38 chr15: 25,213,315-25,213,456 , GRCh37.p13 chr15: 25,458,462-25,458,603 SNORD115-24, SNHG14
    nsv5557813sequence alteration1nstd206human GRCh38 chr15: 23,786,776-25,754,615 , GRCh37.p13 chr15: 24,031,923-25,999,762 , IPW, 110 more genes
    nsv5498998copy number variation1nstd206human GRCh38 chr15: 25,213,050-25,214,382 , GRCh37.p13 chr15: 25,458,197-25,459,529 SNORD115-24, SNORD115-25, 1 more genes
    nsv5496117copy number variation1nstd206human GRCh38 chr15: 25,213,315-25,213,458 , GRCh37.p13 chr15: 25,458,462-25,458,605 SNORD115-24, SNHG14
    nsv5381773copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-27,193,380 , GRCh38.p12 chr15: 23,319,714-26,948,233 SNORD116-5, NPAP1, 139 more genes
    nsv5357721translocation1nstd200human GRCh38 chr15: 25,213,458-25,213,458 , GRCh38 chr15: 25,213,315-25,213,315 , GRCh37.p13 chr15: 25,458,605-25,458,605 , GRCh37.p13 chr15: 25,458,462-25,458,462 SNHG14, SNORD115-24
    nsv5357720translocation1nstd200human GRCh38 chr15: 25,213,050-25,213,050 , GRCh38 chr15: 25,214,382-25,214,382 , GRCh37.p13 chr15: 25,459,529-25,459,529 , GRCh37.p13 chr15: 25,458,197-25,458,197 SNORD115-25, SNORD115-24, 1 more genes
    nsv5342811translocation1nstd200human GRCh37 chr15: 25,458,605-25,458,605 , GRCh37 chr15: 25,458,462-25,458,462 , GRCh38.p12 chr15: 25,213,458-25,213,458 , GRCh38.p12 chr15: 25,213,315-25,213,315 SNHG14, SNORD115-24
    nsv5305433copy number variation1nstd204human GRCh37.p13 chr15: 25,458,457-25,458,609 , GRCh38.p13 chr15: 25,213,310-25,213,462 SNHG14, SNORD115-24
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5060035copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,707,435-28,726,651 , GRCh38.p12 chr15: 23,462,288-28,481,505 PWAR4, SNORD116-18, 150 more genes
    nsv4855601copy number variation1nstd200human GRCh37 chr15: 25,458,643-25,470,113 , GRCh38.p12 chr15: 25,213,496-25,224,966 SNORD115-25, SNORD115-26, 6 more genes
    nsv4855600copy number variation1nstd200human GRCh37 chr15: 25,458,197-25,459,529 , GRCh38.p12 chr15: 25,213,050-25,214,382 SNORD115-24, SNHG14, 1 more genes
    nsv4747663copy number variation1nstd199human GRCh37 chr15: 25,458,461-25,458,602 , GRCh38.p12 chr15: 25,213,314-25,213,455 SNHG14, SNORD115-24
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