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Items: 1 to 20 of 1526

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128289copy number variation1nstd186human GRCh37 chr22: 41,870,367-41,870,673 , GRCh38.p12 chr22: 41,474,363-41,474,669 ACO2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5970058insertion1nstd209human GRCh38 chr20: 2,659,082-2,659,082 , GRCh37.p13 chr20: 2,639,728-2,639,728 IDH3B
    nsv5962194copy number variation1nstd209human GRCh38 chr22: 41,485,461-41,486,503 , GRCh37.p13 chr22: 41,881,465-41,882,507 ACO2
    nsv5946915copy number variation1nstd209human GRCh38 chr12: 56,292,270-56,292,775 , GRCh37.p13 chr12: 56,686,054-56,686,559 CS
    nsv5945363copy number variation1nstd209human GRCh38 chr12: 56,279,724-56,279,925 , GRCh37.p13 chr12: 56,673,508-56,673,709 CS
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5926989copy number variation1nstd209human GRCh38 chr9: 32,420,100-32,420,168 , GRCh37.p13 chr9: 32,420,098-32,420,166 ACO1
    nsv5872951copy number variation1nstd209human GRCh38 chr22: 41,485,406-41,487,919 , GRCh37.p13 chr22: 41,881,410-41,883,923 ACO2
    nsv5718737mobile element insertion1nstd211human GRCh38 chr12: 56,279,356-56,279,356 , GRCh37.p13 chr12: 56,673,140-56,673,140 CS
    nsv5715192mobile element insertion1nstd211human GRCh38 chr22: 41,513,347-41,513,347 , GRCh37.p13 chr22: 41,909,351-41,909,351 ACO2
    nsv5713505mobile element insertion2nstd211human GRCh38 chr9: 32,386,792-32,386,792 , GRCh37.p13 chr9: 32,386,790-32,386,790 ACO1
    nsv5702964mobile element insertion1nstd211human GRCh38 chr9: 32,420,445-32,420,445 , GRCh37.p13 chr9: 32,420,443-32,420,443 ACO1
    nsv5648112insertion1nstd207human GRCh38 chr20: 2,659,082-2,659,082 , GRCh37.p13 chr20: 2,639,728-2,639,728 IDH3B
    nsv5630728insertion1nstd207human GRCh38 chr9: 32,450,936-32,450,936 , GRCh37.p13 chr9: 32,450,934-32,450,934 ACO1
    nsv5629519insertion1nstd207human GRCh38 chr9: 32,420,100-32,420,100 , GRCh37.p13 chr9: 32,420,098-32,420,098 ACO1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5559867mobile element insertion1nstd206human GRCh38 chr12: 56,279,356-56,279,407 , GRCh37.p13 chr12: 56,673,140-56,673,191 CS
    nsv5556515sequence alteration1nstd206human GRCh38 chr15: 77,975,462-78,778,174 , GRCh37.p13 chr15: 78,267,804-79,070,516 , CHRNA5, 26 more genes
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