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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112908copy number variation1nstd186human GRCh37 chrX: 64,240,871-64,241,716 , GRCh38.p12 chrX: 65,020,991-65,021,836 ZC4H2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5874729copy number variation1nstd209human GRCh38 chrX: 64,946,397-64,946,746 , GRCh37.p13 chrX: 64,166,277-64,166,626 ZC4H2
    nsv5870183copy number variation1nstd209human GRCh38 chrX: 65,020,991-65,021,925 , GRCh37.p13 chrX: 64,240,871-64,241,805 ZC4H2
    nsv5672028copy number variation1nstd207human GRCh38 chrX: 65,020,934-65,021,770 , GRCh37.p13 chrX: 64,240,814-64,241,650 ZC4H2
    nsv5620233insertion1nstd207human GRCh38 chrX: 64,954,372-64,954,372 , GRCh37.p13 chrX: 64,174,252-64,174,252 ZC4H2
    nsv5564509copy number variation1nstd102humanPathogenic GRCh37 chrX: 64,166,588-64,361,318 , GRCh38.p12 chrX: 64,946,708-65,141,438 ZC3H12B, ZC4H2
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5428725copy number variation1nstd206human GRCh38 chrX: 65,020,991-65,021,836 , GRCh37.p13 chrX: 64,240,871-64,241,716 ZC4H2
    nsv5417924copy number variation1nstd206human GRCh38 chrX: 64,946,397-64,946,750 , GRCh37.p13 chrX: 64,166,277-64,166,630 ZC4H2
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5384707copy number variation1nstd186human GRCh37 chrX: 64,240,815-64,241,704 , GRCh38.p12 chrX: 65,020,935-65,021,824 ZC4H2
    nsv5376371translocation1nstd200human GRCh38 chrX: 64,946,397-64,946,397 , GRCh38 chrX: 64,946,750-64,946,750 , GRCh37.p13 chrX: 64,166,277-64,166,277 , GRCh37.p13 chrX: 64,166,630-64,166,630 ZC4H2
    nsv5338553translocation1nstd200human GRCh37 chrX: 64,166,277-64,166,277 , GRCh37 chrX: 64,166,630-64,166,630 , GRCh38.p12 chrX: 64,946,750-64,946,750 , GRCh38.p12 chrX: 64,946,397-64,946,397 ZC4H2
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4909045copy number variation1nstd200human GRCh38 chrX: 64,143,653-64,914,249 , GRCh37.p13 chrX: 63,363,533-64,134,129 SHC1P1, LOC105373239, 12 more genes
    nsv4902818copy number variation1nstd200human GRCh38 chrX: 64,995,782-64,997,635 , GRCh37.p13 chrX: 64,215,662-64,217,515 ZC4H2
    nsv4782064copy number variation1nstd200human GRCh37 chrX: 63,363,533-64,134,129 , GRCh38.p12 chrX: 64,143,653-64,914,249 KPNA4P1, KRT8P27, 12 more genes
    nsv4779830copy number variation1nstd200human GRCh37 chrX: 64,240,813-64,241,706 , GRCh38.p12 chrX: 65,020,933-65,021,826 ZC4H2
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