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Items: 1 to 20 of 327

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948576insertion1nstd209human GRCh38 chr6: 36,834,278-36,834,278 , GRCh37.p13 chr6: 36,802,054-36,802,054 CPNE5, C6orf89
    nsv5903496copy number variation1nstd209human GRCh38 chr6: 36,907,628-36,907,711 , GRCh37.p13 chr6: 36,875,404-36,875,487 C6orf89
    nsv5903425copy number variation1nstd209human GRCh38 chr6: 36,921,693-36,921,747 , GRCh37.p13 chr6: 36,889,469-36,889,523 C6orf89
    nsv5903400copy number variation1nstd209human GRCh38 chr6: 36,900,345-36,900,642 , GRCh37.p13 chr6: 36,868,121-36,868,418 C6orf89
    nsv5684295mobile element insertion1nstd211human GRCh38 chr6: 36,854,413-36,854,413 , GRCh37.p13 chr6: 36,822,189-36,822,189 C6orf89, PPIL1
    nsv5552242insertion1nstd206human GRCh38 chr6: 36,925,402-36,925,402 , GRCh37.p13 chr6: 36,893,178-36,893,178 C6orf89
    nsv5470893copy number variation1nstd206human GRCh38 chr6: 36,898,120-36,898,594 , GRCh37.p13 chr6: 36,865,896-36,866,370 C6orf89
    nsv5462845copy number variation1nstd206human GRCh38 chr6: 36,888,745-36,888,922 , GRCh37.p13 chr6: 36,856,521-36,856,698 C6orf89
    nsv5454106copy number variation1nstd206human GRCh38 chr6: 36,921,697-36,921,748 , GRCh37.p13 chr6: 36,889,473-36,889,524 C6orf89
    nsv5406355mobile element insertion1nstd206human GRCh38 chr6: 36,854,413-36,854,464 , GRCh37.p13 chr6: 36,822,189-36,822,240 C6orf89, PPIL1
    nsv5317588copy number variation1nstd204human GRCh38.p13 chr6: 36,902,202-36,902,862 , GRCh37.p13 chr6: 36,869,978-36,870,638 C6orf89
    nsv5317518copy number variation1nstd204human GRCh37.p13 chr6: 36,802,532-36,803,762 , GRCh38.p13 chr6: 36,834,756-36,835,986 CPNE5, C6orf89
    nsv5309894copy number variation1nstd204human GRCh37.p13 chr6: 36,798,984-36,803,252 , GRCh38.p13 chr6: 36,831,208-36,835,476 CPNE5, C6orf89
    nsv5236832copy number variation1nstd204human GRCh38.p13 chr6: 36,831,552-36,835,633 , GRCh37.p13 chr6: 36,799,328-36,803,409 CPNE5, C6orf89
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5108287mobile element insertion1nstd203human GRCh38 chr6: 36,875,245-36,875,250 , GRCh37.p13 chr6: 36,843,021-36,843,026 C6orf89, PPIL1
    nsv5108160mobile element insertion1nstd203human GRCh38 chr6: 36,900,525-36,900,561 , GRCh37.p13 chr6: 36,868,301-36,868,337 C6orf89
    nsv5103864mobile element insertion1nstd203human GRCh38 chr6: 36,900,524-36,900,561 , GRCh37.p13 chr6: 36,868,300-36,868,337 C6orf89
    nsv5102699mobile element insertion1nstd203human GRCh38 chr6: 36,900,561-36,900,600 , GRCh37.p13 chr6: 36,868,337-36,868,376 C6orf89
    nsv5100450mobile element insertion1nstd203human GRCh38 chr6: 36,901,321-36,901,352 , GRCh37.p13 chr6: 36,869,097-36,869,128 C6orf89
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