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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965307insertion1nstd209human GRCh38 chr10: 11,842,931-11,842,931 , GRCh37.p13 chr10: 11,884,930-11,884,930 PROSER2
    nsv5962635insertion1nstd209human GRCh38 chr10: 11,849,102-11,849,102 , GRCh37.p13 chr10: 11,891,101-11,891,101 PROSER2-AS1, PROSER2
    nsv5728583mobile element insertion1nstd211human GRCh38 chr10: 11,840,124-11,840,124 , GRCh37.p13 chr10: 11,882,123-11,882,123 PROSER2
    nsv5700099mobile element insertion1nstd211human GRCh38 chr10: 11,840,529-11,840,529 , GRCh37.p13 chr10: 11,882,528-11,882,528 PROSER2
    nsv5698602mobile element insertion1nstd211human GRCh38 chr10: 11,833,256-11,833,256 , GRCh37.p13 chr10: 11,875,255-11,875,255 PROSER2
    nsv5641391insertion1nstd207human GRCh38 chr10: 11,845,259-11,845,259 , GRCh37.p13 chr10: 11,887,258-11,887,258 PROSER2
    nsv5629791insertion1nstd207human GRCh38 chr10: 11,839,695-11,839,695 , GRCh37.p13 chr10: 11,881,694-11,881,694 PROSER2
    nsv5549449insertion1nstd206human GRCh38 chr10: 11,849,102-11,849,102 , GRCh37.p13 chr10: 11,891,101-11,891,101 PROSER2, PROSER2-AS1
    nsv5491231copy number variation1nstd206human GRCh38 chr10: 11,832,797-11,833,142 , GRCh37.p13 chr10: 11,874,796-11,875,141 PROSER2
    nsv5484874copy number variation1nstd206human GRCh38 chr10: 11,853,324-11,856,766 , GRCh37.p13 chr10: 11,895,323-11,898,765 PROSER2, PROSER2-AS1
    nsv5479321copy number variation1nstd206human GRCh38 chr10: 11,805,142-11,860,066 , GRCh37.p13 chr10: 11,847,141-11,902,065 PROSER2-AS1, PROSER2
    nsv5403852mobile element insertion1nstd206human GRCh38 chr10: 11,840,529-11,840,580 , GRCh37.p13 chr10: 11,882,528-11,882,579 PROSER2
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5330949translocation1nstd200human GRCh37 chr10: 11,883,078-11,883,078 , GRCh37 chr10: 11,882,650-11,882,650 , GRCh38.p12 chr10: 11,840,651-11,840,651 , GRCh38.p12 chr10: 11,841,079-11,841,079 PROSER2
    nsv5250786copy number variation1nstd204human GRCh38.p13 chr10: 11,855,501-12,052,400 , GRCh37.p13 chr10: 11,897,500-12,094,399 LOC105376416, UPF2, 3 more genes
    nsv5245875copy number variation1nstd204human GRCh38.p13 chr10: 11,860,126-11,884,902 , GRCh37.p13 chr10: 11,902,125-11,926,901 PROSER2-AS1, PROSER2
    nsv5206385mobile element deletion1nstd204human GRCh38.p13 chr10: 11,832,844-11,833,151 , GRCh37.p13 chr10: 11,874,843-11,875,150 PROSER2
    nsv5199123mobile element insertion1nstd203human GRCh38 chr10: 11,831,068-11,831,085 , GRCh37.p13 chr10: 11,873,067-11,873,084 PROSER2
    nsv5130391mobile element insertion1nstd203human GRCh38 chr10: 11,842,953-11,842,958 , GRCh37.p13 chr10: 11,884,952-11,884,957 PROSER2
    nsv5123193mobile element insertion1nstd203human GRCh38 chr10: 11,849,060-11,849,110 , GRCh37.p13 chr10: 11,891,059-11,891,109 PROSER2, PROSER2-AS1
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