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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7030438copy number variation1nstd229human GRCh38 chr20: 32,825,917-32,828,432 , GRCh37.p13 chr20: 31,413,723-31,416,238 MAPRE1
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6596546inversion1nstd223human GRCh38 chr20: 32,825,512-32,826,236 , GRCh37.p13 chr20: 31,413,318-31,414,042 MAPRE1
    nsv6595836inversion1nstd223human GRCh38 chr20: 32,826,240-32,827,368 , GRCh37.p13 chr20: 31,414,046-31,415,174 MAPRE1
    nsv6532251copy number variation1nstd223human GRCh38 chr20: 32,812,801-32,818,300 , GRCh37.p13 chr20: 31,400,607-31,406,106 MAPRE1
    nsv6524898copy number variation1nstd223human GRCh38 chr20: 32,842,425-32,844,541 , GRCh37.p13 chr20: 31,430,231-31,432,347 MAPRE1
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134020copy number variation1nstd213human GRCh37 chr20: 31,320,000-31,470,001 , GRCh38.p12 chr20: 32,732,193-32,882,195 DNMT3B, MAPRE1, 2 more genes
    nsv6133806copy number variation1nstd213human GRCh37 chr20: 30,990,000-32,330,001 , GRCh38.p12 chr20: 32,402,197-33,742,195 SNTA1, ZNF341, 36 more genes
    nsv5705931mobile element insertion1nstd211human GRCh38 chr20: 32,831,964-32,831,964 , GRCh37.p13 chr20: 31,419,770-31,419,770 MAPRE1
    nsv5699418mobile element insertion1nstd211human GRCh38 chr20: 32,835,380-32,835,380 , GRCh37.p13 chr20: 31,423,186-31,423,186 MAPRE1
    nsv5533282copy number variation1nstd206human GRCh38 chr20: 32,840,985-32,843,973 , GRCh37.p13 chr20: 31,428,791-31,431,779 MAPRE1
    nsv5532530copy number variation1nstd206human GRCh38 chr20: 32,838,494-32,838,569 , GRCh37.p13 chr20: 31,426,300-31,426,375 MAPRE1
    nsv5350298translocation1nstd200human GRCh38 chr20: 32,826,049-32,826,049 , GRCh38 chr20: 32,833,712-32,833,712 , GRCh37.p13 chr20: 31,413,855-31,413,855 , GRCh37.p13 chr20: 31,421,518-31,421,518 MAPRE1
    nsv5321093copy number variation1nstd204human GRCh38.p13 chr20: 32,820,425-32,824,947 , GRCh37.p13 chr20: 31,408,231-31,412,753 MAPRE1
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