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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7060373inversion1nstd229human GRCh38 chr20: 44,723,151-44,723,233 , GRCh37.p13 chr20: 43,351,792-43,351,874 KCNK15-AS1, CCN5
    nsv7034451copy number variation1nstd229human GRCh38 chr20: 44,718,876-44,780,373 , GRCh37.p13 chr20: 43,347,517-43,409,014 KCNK15, CCN5, 2 more genes
    nsv7032643copy number variation1nstd229human GRCh38 chr20: 44,734,370-44,734,437 , GRCh37.p13 chr20: 43,363,011-43,363,078 KCNK15-AS1
    nsv7031703copy number variation1nstd229human GRCh38 chr20: 44,714,280-44,719,850 , GRCh37.p13 chr20: 43,342,921-43,348,491 KCNK15-AS1, CCN5
    nsv7030029copy number variation1nstd229human GRCh38 chr20: 44,719,401-44,721,900 , GRCh37.p13 chr20: 43,348,042-43,350,541 KCNK15-AS1, CCN5
    nsv7028741copy number variation1nstd229human GRCh38 chr20: 44,719,345-44,726,389 , GRCh37.p13 chr20: 43,347,986-43,355,030 CCN5, KCNK15-AS1
    nsv7020922copy number variation1nstd229human GRCh38 chr20: 44,733,384-44,738,918 , GRCh37.p13 chr20: 43,362,025-43,367,559 KCNK15-AS1
    nsv7018373copy number variation1nstd229human GRCh38 chr20: 44,720,114-44,727,084 , GRCh37.p13 chr20: 43,348,755-43,355,725 KCNK15-AS1, CCN5
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6553230copy number variation1nstd223human GRCh38 chr20: 44,719,342-44,726,389 , GRCh37.p13 chr20: 43,347,983-43,355,030 KCNK15-AS1, CCN5
    nsv6551255copy number variation1nstd223human GRCh38 chr20: 44,711,489-44,713,756 , GRCh37.p13 chr20: 43,340,130-43,342,397 KCNK15-AS1, CCN5
    nsv6539333copy number variation1nstd223human GRCh38 chr20: 44,725,812-44,731,370 , GRCh37.p13 chr20: 43,354,453-43,360,011 KCNK15-AS1, CCN5
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6134297copy number variation1nstd213human GRCh37 chr20: 42,590,000-43,450,001 , GRCh38.p12 chr20: 43,961,360-44,821,360 ADA, OSER1, 22 more genes
    nsv6134164copy number variation1nstd213human GRCh37 chr20: 43,170,000-44,070,001 , GRCh38.p12 chr20: 44,541,359-45,441,361 PI3, SEMG2, 35 more genes
    nsv6103346insertion1nstd212human GRCh38 chr20: 44,745,397-44,745,397 , GRCh37.p13 chr20: 43,374,038-43,374,038 KCNK15-AS1, KCNK15
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5667153insertion1nstd207human GRCh38 chr20: 44,745,387-44,745,387 , GRCh37.p13 chr20: 43,374,028-43,374,028 KCNK15, KCNK15-AS1
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