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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098462copy number variation1nstd102humanPathogenic GRCh37 chr9: 3,828,272-5,126,791 , GRCh38.p12 chr9: 3,828,272-5,126,791 AK3, TCF3P1, 30 more genes
    nsv7073649inversion1nstd229human GRCh38 chr9: 4,659,571-5,011,425 , GRCh37.p13 chr9: 4,659,571-5,011,425 RCL1, CDC37L1, 11 more genes
    nsv7071567inversion1nstd229human GRCh38 chr9: 4,825,757-4,832,874 , GRCh37.p13 chr9: 4,825,757-4,832,874 RCL1
    nsv7066230inversion1nstd229human GRCh38 chr9: 235,930-9,843,002 , GRCh37.p13 chr9: 235,930-9,843,002 GLIS3-AS1, LOC105375955, 118 more genes
    nsv6877416copy number variation1nstd229human GRCh38 chr9: 4,735,655-4,793,169 , GRCh37.p13 chr9: 4,735,655-4,793,169 RPS5P6, RCL1, 2 more genes
    nsv6876355copy number variation1nstd229human GRCh38 chr9: 4,773,300-5,092,659 , GRCh37.p13 chr9: 4,773,300-5,092,659 RCL1, PDSS1P1, 10 more genes
    nsv6876292copy number variation1nstd229human GRCh38 chr9: 4,816,801-4,820,000 , GRCh37.p13 chr9: 4,816,801-4,820,000 RCL1
    nsv6874289copy number variation1nstd229human GRCh38 chr9: 4,797,901-4,814,300 , GRCh37.p13 chr9: 4,797,901-4,814,300 KLF4P1, RCL1
    nsv6874127copy number variation1nstd229human GRCh38 chr9: 4,801,559-4,806,218 , GRCh37.p13 chr9: 4,801,559-4,806,218 KLF4P1, RCL1
    nsv6873097copy number variation1nstd229human GRCh38 chr9: 4,664,051-4,822,692 , GRCh37.p13 chr9: 4,664,051-4,822,692 CDC37L1-DT, RCL1, 7 more genes
    nsv6873082copy number variation1nstd229human GRCh38 chr9: 4,814,309-4,886,626 , GRCh37.p13 chr9: 4,814,309-4,886,626 MIR101-2, RCL1
    nsv6869135copy number variation1nstd229human GRCh38 chr9: 4,737,429-4,792,677 , GRCh37.p13 chr9: 4,737,429-4,792,677 RCL1, ECM1P1, 2 more genes
    nsv6868145copy number variation1nstd229human GRCh38 chr9: 4,606,225-4,820,320 , GRCh37.p13 chr9: 4,606,225-4,820,320 CDC37L1, ECM1P1, 8 more genes
    nsv6867256copy number variation1nstd229human GRCh38 chr9: 4,775,201-4,792,000 , GRCh37.p13 chr9: 4,775,201-4,792,000 RPS5P6, RCL1
    nsv6864617copy number variation1nstd229human GRCh38 chr9: 4,830,327-4,836,944 , GRCh37.p13 chr9: 4,830,327-4,836,944 RCL1
    nsv6863892copy number variation1nstd229human GRCh38 chr9: 4,625,116-5,645,668 , GRCh37.p13 chr9: 4,625,116-5,645,668 INSL6, TCF3P1, 33 more genes
    nsv6859028copy number variation1nstd229human GRCh38 chr9: 4,713,801-4,942,500 , GRCh37.p13 chr9: 4,713,801-4,942,500 MIR101-2, AK3, 5 more genes
    nsv6858968copy number variation1nstd229human GRCh38 chr9: 4,733,401-4,800,800 , GRCh37.p13 chr9: 4,733,401-4,800,800 AK3, ECM1P1, 2 more genes
    nsv6638036copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 203,862-5,958,840 , GRCh38.p12 chr9: 203,862-5,958,840 DMRT1, MLANA, 86 more genes
    nsv6637634copy number variation1nstd102humanUncertain significance GRCh37 chr9: 4,386,288-5,003,101 , GRCh38.p12 chr9: 4,386,288-5,003,101 MIR101-2, PLPP6, 14 more genes
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