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Items: 1 to 20 of 492

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3882191copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,331,686-50,332,367 , GRCh38 chr19: 49,828,429-49,829,110 MED25
    nsv6507622copy number variation1nstd223human GRCh38 chr17: 17,483,859-17,490,307 , GRCh37.p13 chr17: 17,387,173-17,393,621 MED9
    nsv6504205copy number variation1nstd223human GRCh38 chr17: 17,471,749-17,476,473 , GRCh37.p13 chr17: 17,375,063-17,379,787 MED9
    nsv6517482copy number variation1nstd223human GRCh38 chr19: 49,821,570-49,826,068 , GRCh37.p13 chr19: 50,324,827-50,329,325 MED25
    nsv6501535copy number variation1nstd223human GRCh38 chr17: 17,481,201-17,483,300 , GRCh37.p13 chr17: 17,384,515-17,386,614 MED9
    nsv6519347copy number variation1nstd223human GRCh38 chr19: 49,821,777-49,822,224 , GRCh37.p13 chr19: 50,325,034-50,325,481 MED25
    nsv5525195copy number variation1nstd206human GRCh38 chr19: 49,821,777-49,822,224 , GRCh37.p13 chr19: 50,325,034-50,325,481 MED25
    nsv6128431copy number variation1nstd186human GRCh37 chr19: 50,325,034-50,325,481 , GRCh38.p12 chr19: 49,821,777-49,822,224 MED25
    nsv6051462copy number variation1nstd212human GRCh38 chr19: 49,822,711-49,822,909 , GRCh37.p13 chr19: 50,325,968-50,326,166 MED25
    nsv6050195copy number variation1nstd212human GRCh38 chr19: 49,822,851-49,822,940 , GRCh37.p13 chr19: 50,326,108-50,326,197 MED25
    nsv4706837copy number variation1nstd195human GRCh37 chr19: 50,325,034-50,325,035 , GRCh38.p12 chr19: 49,821,777-49,821,778 MED25
    nsv4739792copy number variation1nstd199human GRCh37 chr19: 50,325,959-50,326,060 , GRCh38.p12 chr19: 49,822,702-49,822,803 MED25
    nsv5328120copy number variation1nstd204human GRCh38.p13 chr19: 49,821,800-49,822,259 , GRCh37.p13 chr19: 50,325,057-50,325,516 MED25
    nsv5026122copy number variation1nstd200human GRCh38 chr17: 17,483,887-17,490,324 , GRCh37.p13 chr17: 17,387,201-17,393,638 MED9
    nsv4858245copy number variation1nstd200human GRCh37 chr17: 17,387,214-17,393,621 , GRCh38.p12 chr17: 17,483,900-17,490,307 MED9
    nsv5021009copy number variation1nstd200human GRCh38 chr19: 49,822,066-49,827,957 , GRCh37.p13 chr19: 50,325,323-50,331,214 MED25
    nsv5026121copy number variation1nstd200human GRCh38 chr17: 17,481,066-17,483,697 , GRCh37.p13 chr17: 17,384,380-17,387,011 MED9
    nsv5947278copy number variation1nstd209human GRCh38 chr19: 49,821,777-49,822,223 , GRCh37.p13 chr19: 50,325,034-50,325,480 MED25
    nsv5944129copy number variation1nstd209human GRCh38 chr19: 49,821,493-49,821,677 , GRCh37.p13 chr19: 50,324,750-50,324,934 MED25
    nsv4237793copy number variation1nstd166human GRCh37.p13 chr17: 17,387,174-17,393,621 , GRCh38.p12 chr17: 17,483,860-17,490,307 MED9
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