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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962635insertion1nstd209human GRCh38 chr10: 11,849,102-11,849,102 , GRCh37.p13 chr10: 11,891,101-11,891,101 PROSER2-AS1, PROSER2
    nsv5912155copy number variation1nstd209human GRCh38 chr10: 11,885,322-11,885,516 , GRCh37.p13 chr10: 11,927,321-11,927,515 PROSER2-AS1
    nsv5642450insertion1nstd207human GRCh38 chr10: 11,885,296-11,885,296 , GRCh37.p13 chr10: 11,927,295-11,927,295 PROSER2-AS1
    nsv5637873insertion3nstd207human GRCh38 chr10: 11,885,400-11,885,400 , GRCh37.p13 chr10: 11,927,399-11,927,399 PROSER2-AS1
    nsv5593551copy number variation1nstd207human GRCh38 chr10: 11,885,356-11,885,472 , GRCh37.p13 chr10: 11,927,355-11,927,471 PROSER2-AS1
    nsv5549449insertion1nstd206human GRCh38 chr10: 11,849,102-11,849,102 , GRCh37.p13 chr10: 11,891,101-11,891,101 PROSER2, PROSER2-AS1
    nsv5484874copy number variation1nstd206human GRCh38 chr10: 11,853,324-11,856,766 , GRCh37.p13 chr10: 11,895,323-11,898,765 PROSER2, PROSER2-AS1
    nsv5479574copy number variation1nstd206human GRCh38 chr10: 11,893,544-11,893,633 , GRCh37.p13 chr10: 11,935,543-11,935,632 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
    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
    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
    nsv5125158mobile element insertion1nstd203human GRCh38 chr10: 11,879,204-11,879,215 , GRCh37.p13 chr10: 11,921,203-11,921,214 PROSER2-AS1
    nsv5123193mobile element insertion1nstd203human GRCh38 chr10: 11,849,060-11,849,110 , GRCh37.p13 chr10: 11,891,059-11,891,109 PROSER2, PROSER2-AS1
    nsv4983742copy number variation1nstd200human GRCh38 chr10: 11,848,864-11,930,625 , GRCh37.p13 chr10: 11,890,863-11,972,624 UPF2, RNU6-1095P, 2 more genes
    nsv4974913copy number variation1nstd200human GRCh38 chr10: 11,892,785-11,907,451 , GRCh37.p13 chr10: 11,934,784-11,949,450 PROSER2-AS1
    nsv4974912copy number variation1nstd200human GRCh38 chr10: 11,890,622-11,900,580 , GRCh37.p13 chr10: 11,932,621-11,942,579 PROSER2-AS1
    nsv4974911copy number variation1nstd200human GRCh38 chr10: 11,859,737-11,864,085 , GRCh37.p13 chr10: 11,901,736-11,906,084 PROSER2-AS1, PROSER2
    nsv4974910copy number variation1nstd200human GRCh38 chr10: 11,852,811-11,854,571 , GRCh37.p13 chr10: 11,894,810-11,896,570 PROSER2, PROSER2-AS1
    nsv4974909copy number variation1nstd200human GRCh38 chr10: 11,848,954-11,853,316 , GRCh37.p13 chr10: 11,890,953-11,895,315 PROSER2, PROSER2-AS1
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