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Items: 1 to 20 of 1232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116675mobile element insertion1nstd186human GRCh37 chr7: 143,153,580-143,153,631 , GRCh38.p12 chr7|NW_018654714.1: 75,851-75,902 , GRCh38.p12 chr7: 143,456,487-143,456,538 EPHA1-AS1
    nsv5387516copy number variation1nstd186human GRCh37 chr7: 143,721,194-143,721,397 , GRCh38.p12 chr7|NW_018654714.1: 568,331-568,534 , GRCh38.p12 chr7: 144,024,101-144,024,304 0
    nsv4827278copy number variation1nstd200human GRCh37 chr7: 143,737,508-143,742,912 , GRCh38.p12 chr7|NW_018654714.1: 584,645-589,657 , GRCh38.p12 chr7: 144,040,415-144,045,819 0
    nsv4827277copy number variation1nstd200human GRCh37 chr7: 143,712,809-143,719,305 , GRCh38.p12 chr7: 144,015,716-144,022,212 , GRCh38.p12 chr7|NW_018654714.1: 559,946-566,442 0
    nsv4827276copy number variation1nstd200human GRCh37 chr7: 143,684,866-143,690,366 , GRCh38.p12 chr7|NW_018654714.1: 532,003-537,503 , GRCh38.p12 chr7: 143,987,773-143,993,273 OR2F1
    nsv4827275copy number variation1nstd200human GRCh37 chr7: 143,637,825-143,638,056 , GRCh38.p12 chr7: 143,940,732-143,940,963 , GRCh38.p12 chr7|NW_018654714.1: 484,960-485,191 OR2F1
    nsv4827274copy number variation1nstd200human GRCh37 chr7: 143,432,840-143,432,956 , GRCh38.p12 chr7|NW_018654714.1: 280,067-280,183 , GRCh38.p12 chr7: 143,735,747-143,735,863 0
    nsv4827273copy number variation1nstd200human GRCh37 chr7: 143,204,809-143,206,693 , GRCh38.p12 chr7: 143,507,716-143,509,600 , GRCh38.p12 chr7|NW_018654714.1: 127,080-128,964 EPHA1-AS1, OR10AC1
    nsv4827272copy number variation1nstd200human GRCh37 chr7: 143,166,295-143,166,387 , GRCh38.p12 chr7: 143,469,202-143,469,294 , GRCh38.p12 chr7|NW_018654714.1: 88,566-88,658 EPHA1-AS1
    nsv4827271copy number variation1nstd200human GRCh37 chr7: 143,154,420-143,184,033 , GRCh38.p12 chr7: 143,457,327-143,486,940 , GRCh38.p12 chr7|NW_018654714.1: 76,691-106,304 OR2R1P, EPHA1-AS1, 1 more genes
    nsv4825402copy number variation1nstd200human GRCh37 chr7: 143,660,195-143,699,177 , GRCh38.p12 chr7: 143,963,102-144,002,084 , GRCh38.p12 chr7|NW_018654714.1: 507,332-546,314 CAPZA1P5, SLC16A1P1, 3 more genes
    nsv4787374mobile element deletion1nstd200human GRCh37 chr7: 143,737,788-143,738,045 , GRCh38.p12 chr7|NW_018654714.1: 584,925-585,182 , GRCh38.p12 chr7: 144,040,695-144,040,952 0
    nsv4763948insertion1nstd199human GRCh37 chr7: 143,721,220-143,721,220 , GRCh38.p12 chr7: 144,024,127-144,024,127 , GRCh38.p12 chr7|NW_018654714.1: 568,357-568,357 0
    nsv4763416insertion1nstd199human GRCh37 chr7: 143,220,055-143,220,055 , GRCh38.p12 chr7: 143,522,962-143,522,962 , GRCh38.p12 chr7|NW_018654714.1: 142,326-142,326 EPHA1-AS1
    nsv4758146insertion1nstd199human GRCh37 chr7: 143,603,545-143,603,545 , GRCh38.p12 chr7|NW_018654714.1: 450,680-450,680 , GRCh38.p12 chr7: 143,906,452-143,906,452 OR2F1
    nsv4724782insertion1nstd186human GRCh37 chr7: 143,153,563-143,153,563 , GRCh38.p12 chr7|NW_018654714.1: 75,834-75,834 , GRCh38.p12 chr7: 143,456,470-143,456,470 EPHA1-AS1
    nsv4713521copy number variation1nstd195human GRCh37 chr7: 143,226,601-143,227,851 , GRCh38.p12 chr7: 143,529,508-143,530,758 , GRCh38.p12 chr7|NW_018654714.1: 148,872-150,122 RPL26P22
    nsv4711640copy number variation1nstd195human GRCh37 chr7: 143,647,529-143,647,530 , GRCh38.p12 chr7|NW_018654714.1: 494,666-494,667 , GRCh38.p12 chr7: 143,950,436-143,950,437 OR2F1
    nsv4709749translocation1nstd195human GRCh37 chr7: 143,640,998-143,640,998 , GRCh37 chr12: 44,931,166-44,931,166 , GRCh38.p12 chr12: 44,537,383-44,537,383 , GRCh38.p12 chr7: 143,943,905-143,943,905 , GRCh38.p12 chr7|NW_018654714.1: 488,133-488,133 NELL2, OR2F1
    nsv4707568translocation1nstd195human GRCh37 chr7: 143,640,997-143,640,997 , GRCh37 chr12: 44,931,166-44,931,166 , GRCh38.p12 chr12: 44,537,383-44,537,383 , GRCh38.p12 chr7: 143,943,904-143,943,904 , GRCh38.p12 chr7|NW_018654714.1: 488,132-488,132 NELL2, OR2F1
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