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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971875insertion1nstd209human GRCh38 chr15: 42,010,139-42,010,139 , GRCh37.p13 chr15: 42,302,337-42,302,337 PLA2G4E
    nsv5932657copy number variation1nstd209human GRCh38 chr15: 41,987,855-41,987,930 , GRCh37.p13 chr15: 42,280,053-42,280,128 PLA2G4E-AS1, PLA2G4E
    nsv5716435mobile element insertion1nstd211human GRCh38 chr15: 42,040,801-42,040,801 , GRCh37.p13 chr15: 42,332,999-42,332,999 PLA2G4E
    nsv5700580mobile element insertion1nstd211human GRCh38 chr15: 42,035,657-42,035,657 , GRCh37.p13 chr15: 42,327,855-42,327,855 PLA2G4E
    nsv5590887copy number variation1nstd207human GRCh38 chr15: 41,987,855-41,987,930 , GRCh37.p13 chr15: 42,280,053-42,280,128 PLA2G4E, PLA2G4E-AS1
    nsv5558169mobile element insertion1nstd206human GRCh38 chr15: 42,040,801-42,040,829 , GRCh37.p13 chr15: 42,332,999-42,333,027 PLA2G4E, LOC105370793
    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
    nsv5144169mobile element insertion1nstd203human GRCh38 chr15: 42,035,642-42,035,657 , GRCh37.p13 chr15: 42,327,840-42,327,855 PLA2G4E
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005314copy number variation1nstd200human GRCh38 chr15: 42,044,061-42,088,054 , GRCh37.p13 chr15: 42,336,259-42,380,252 LOC105370793, PLA2G4E, 1 more genes
    nsv5001452copy number variation1nstd200human GRCh38 chr15: 42,047,247-42,049,993 , GRCh37.p13 chr15: 42,339,445-42,342,191 PLA2G4E
    nsv5001451copy number variation1nstd200human GRCh38 chr15: 42,021,704-42,026,940 , GRCh37.p13 chr15: 42,313,902-42,319,138 PLA2G4E
    nsv5001450copy number variation1nstd200human GRCh38 chr15: 42,005,346-42,017,062 , GRCh37.p13 chr15: 42,297,544-42,309,260 PLA2G4E
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4729715copy number variation1nstd102humanLikely benign GRCh37 chr15: 41,869,275-42,484,890 , GRCh38.p12 chr15: 41,577,077-42,192,692 SPTBN5, RNA5SP393, 18 more genes
    nsv4628885copy number variation1nstd183human GRCh37 chr15: 42,294,822-42,294,930 , GRCh38.p12 chr15: 42,002,624-42,002,732 PLA2G4E
    nsv4625541copy number variation1nstd183human GRCh37 chr15: 42,149,472-42,309,099 , GRCh38.p12 chr15: 41,857,274-42,016,901 EHD4, SPTBN5, 5 more genes
    nsv4621732copy number variation1nstd183human GRCh37 chr15: 42,156,134-42,638,503 , GRCh38.p12 chr15: 41,863,936-42,346,305 BNIP3P5, PLA2G4D, 14 more genes
    nsv4514528mobile element insertion1nstd166human GRCh37.p13 chr15: 42,327,840-42,327,840 , GRCh38.p12 chr15: 42,035,642-42,035,642 PLA2G4E
    nsv4250845copy number variation1nstd166human GRCh37.p13 chr15: 42,280,054-42,280,129 , GRCh38.p12 chr15: 41,987,856-41,987,931 PLA2G4E, PLA2G4E-AS1
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