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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6969900copy number variation1nstd229human GRCh38 chr15: 41,830,277-41,847,953 , GRCh37.p13 chr15: 42,122,475-42,140,151 PLA2G4B, JMJD7, 2 more genes
    nsv6964218copy number variation1nstd229human GRCh38 chr15: 41,758,370-42,299,821 , GRCh37.p13 chr15: 42,050,568-42,592,019 LOC105370793, RNA5SP393, 19 more genes
    nsv6961462copy number variation1nstd229human GRCh38 chr15: 41,447,415-41,910,191 , GRCh37.p13 chr15: 41,739,613-42,202,389 ELOCP2, EHD4, 18 more genes
    nsv6959873copy number variation1nstd229human GRCh38 chr15: 41,831,427-41,832,835 , GRCh37.p13 chr15: 42,123,625-42,125,033 JMJD7-PLA2G4B, JMJD7
    nsv6959552copy number variation1nstd229human GRCh38 chr15: 41,833,204-41,837,425 , GRCh37.p13 chr15: 42,125,402-42,129,623 JMJD7-PLA2G4B, JMJD7, 1 more genes
    nsv6512698copy number variation1nstd223human GRCh38 chr15: 41,723,075-41,924,332 , GRCh37.p13 chr15: 42,015,273-42,216,530 MGA, RNA5SP393, 9 more genes
    nsv6511877copy number variation1nstd223human GRCh38 chr15: 41,831,401-41,832,700 , GRCh37.p13 chr15: 42,123,599-42,124,898 JMJD7-PLA2G4B, JMJD7
    nsv6508926copy number variation1nstd223human GRCh38 chr15: 41,786,526-42,142,941 , GRCh37.p13 chr15: 42,078,724-42,435,139 EHD4-AS1, PLA2G4B, 13 more genes
    nsv5671848inversion1nstd207human GRCh38 chr15: 41,834,738-41,857,144 , GRCh37.p13 chr15: 42,126,936-42,149,342 JMJD7-PLA2G4B, SPTBN5, 3 more genes
    nsv5500775copy number variation1nstd206human GRCh38 chr15: 41,830,710-41,831,842 , GRCh37.p13 chr15: 42,122,908-42,124,040 JMJD7-PLA2G4B, JMJD7
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5141101mobile element insertion1nstd203human GRCh38 chr15: 41,829,313-41,829,329 , GRCh37.p13 chr15: 42,121,511-42,121,527 JMJD7-PLA2G4B, JMJD7
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001443copy number variation1nstd200human GRCh38 chr15: 41,836,201-41,836,710 , GRCh37.p13 chr15: 42,128,399-42,128,908 JMJD7, JMJD7-PLA2G4B
    nsv5001442copy number variation1nstd200human GRCh38 chr15: 41,831,387-41,832,924 , GRCh37.p13 chr15: 42,123,585-42,125,122 JMJD7, JMJD7-PLA2G4B
    nsv5001441copy number variation1nstd200human GRCh38 chr15: 41,830,710-41,831,842 , GRCh37.p13 chr15: 42,122,908-42,124,040 JMJD7-PLA2G4B, JMJD7
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4865912copy number variation1nstd200human GRCh37 chr15: 42,128,399-42,128,908 , GRCh38.p12 chr15: 41,836,201-41,836,710 JMJD7-PLA2G4B, JMJD7
    nsv4865911copy number variation1nstd200human GRCh37 chr15: 42,123,579-42,124,882 , GRCh38.p12 chr15: 41,831,381-41,832,684 JMJD7-PLA2G4B, JMJD7
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