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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5875438copy number variation1nstd209human GRCh38 chr1: 114,902,451-114,902,813 , GRCh37.p13 chr1: 115,445,072-115,445,434 LOC105378915, SYCP1
    nsv5728263mobile element insertion1nstd211human GRCh38 chr1: 114,861,511-114,861,511 , GRCh37.p13 chr1: 115,404,132-115,404,132 SYCP1
    nsv5716425mobile element insertion2nstd211human GRCh38 chr1: 114,993,183-114,993,183 , GRCh37.p13 chr1: 115,535,804-115,535,804 SYCP1
    nsv5692940mobile element insertion1nstd211human GRCh38 chr1: 114,907,025-114,907,025 , GRCh37.p13 chr1: 115,449,646-115,449,646 SYCP1
    nsv5686393mobile element insertion1nstd211human GRCh38 chr1: 114,992,275-114,992,275 , GRCh37.p13 chr1: 115,534,896-115,534,896 SYCP1
    nsv5675094mobile element insertion1nstd211human GRCh38 chr1: 114,875,201-114,875,201 , GRCh37.p13 chr1: 115,417,822-115,417,822 SYCP1
    nsv5619226insertion1nstd207human GRCh38 chr1: 114,907,011-114,907,011 , GRCh37.p13 chr1: 115,449,632-115,449,632 SYCP1
    nsv5572176copy number variation1nstd207human GRCh38 chr1: 114,902,451-114,902,813 , GRCh37.p13 chr1: 115,445,072-115,445,434 SYCP1, LOC105378915
    nsv5429360copy number variation1nstd206human GRCh38 chr1: 111,687,835-115,150,000 , GRCh37.p13 chr1: 112,230,457-115,692,621 , ST7L, 77 more genes
    nsv5423452copy number variation1nstd206human GRCh38 chr1: 114,870,826-114,870,884 , GRCh37.p13 chr1: 115,413,447-115,413,505 SYCP1
    nsv5422726copy number variation1nstd206human GRCh38 chr1: 114,902,452-114,902,814 , GRCh37.p13 chr1: 115,445,073-115,445,435 SYCP1, LOC105378915
    nsv5421518copy number variation1nstd206human GRCh38 chr1: 114,936,994-114,937,778 , GRCh37.p13 chr1: 115,479,615-115,480,399 SYCP1
    nsv5418323copy number variation1nstd206human GRCh38 chr1: 114,984,024-114,984,119 , GRCh37.p13 chr1: 115,526,645-115,526,740 SYCP1
    nsv5417200copy number variation1nstd206human GRCh38 chr1: 114,911,074-114,911,135 , GRCh37.p13 chr1: 115,453,695-115,453,756 SYCP1
    nsv5397339mobile element insertion1nstd206human GRCh38 chr1: 114,992,275-114,992,326 , GRCh37.p13 chr1: 115,534,896-115,534,947 SYCP1
    nsv5396162mobile element insertion1nstd206human GRCh38 chr1: 114,907,025-114,907,076 , GRCh37.p13 chr1: 115,449,646-115,449,697 SYCP1
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5363420translocation1nstd200human GRCh38 chr1: 114,909,500-114,909,500 , GRCh38 chr1: 114,910,922-114,910,922 , GRCh37.p13 chr1: 115,453,543-115,453,543 , GRCh37.p13 chr1: 115,452,121-115,452,121 SYCP1
    nsv5363419translocation1nstd200human GRCh38 chr12: 21,403,602-21,403,602 , GRCh38 chr1: 114,891,431-114,891,431 , GRCh37.p13 chr12: 21,556,536-21,556,536 , GRCh37.p13 chr1: 115,434,052-115,434,052 SYCP1, SLCO1A2
    nsv5353810translocation1nstd200human GRCh38 chr1: 114,877,739-114,877,739 , GRCh38 chr1: 114,877,793-114,877,793 , GRCh37.p13 chr1: 115,420,360-115,420,360 , GRCh37.p13 chr1: 115,420,414-115,420,414 SYCP1
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