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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
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 more genes
    nsv7063922inversion1nstd229human GRCh38 chr20: 43,626,165-43,772,216 , GRCh37.p13 chr20: 42,254,805-42,400,856 RPL27AP, IFT52, 3 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
    nsv7061700inversion1nstd229human GRCh38 chr20: 43,564,590-43,703,553 , GRCh37.p13 chr20: 42,193,230-42,332,193 SGK2, RPL27AP, 2 more genes
    nsv7038054copy number variation1nstd229human GRCh38 chr20: 43,658,388-43,665,922 , GRCh37.p13 chr20: 42,287,028-42,294,562 MYBL2
    nsv7037840copy number variation1nstd229human GRCh38 chr20: 43,703,601-43,772,200 , GRCh37.p13 chr20: 42,332,241-42,400,840 LOC101927200, GTSF1L, 1 more genes
    nsv7032569copy number variation1nstd229human GRCh38 chr20: 43,631,036-43,692,886 , GRCh37.p13 chr20: 42,259,676-42,321,526 IFT52, RPL27AP, 1 more genes
    nsv7027513copy number variation1nstd229human GRCh38 chr20: 43,716,417-43,716,969 , GRCh37.p13 chr20: 42,345,057-42,345,609 MYBL2
    nsv7023643copy number variation1nstd229human GRCh38 chr20: 43,692,755-43,696,504 , GRCh37.p13 chr20: 42,321,395-42,325,144 MYBL2
    nsv7021263copy number variation1nstd229human GRCh38 chr20: 43,590,311-43,770,924 , GRCh37.p13 chr20: 42,218,951-42,399,564 GTSF1L, MYBL2, 3 more genes
    nsv6626699copy number variation1nstd224human GRCh37 chr20: 42,232,903-42,328,424 , GRCh38.p12 chr20: 43,604,263-43,699,784 IFT52, MYBL2, 1 more genes
    nsv6597889inversion1nstd223human GRCh38 chr20: 43,693,244-43,694,200 , GRCh37.p13 chr20: 42,321,884-42,322,840 MYBL2
    nsv6597672inversion1nstd223human GRCh38 chr20: 43,697,933-43,698,382 , GRCh37.p13 chr20: 42,326,573-42,327,022 MYBL2
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6595913inversion1nstd223human GRCh38 chr20: 43,697,019-43,697,372 , GRCh37.p13 chr20: 42,325,659-42,326,012 MYBL2
    nsv6550900copy number variation1nstd223human GRCh38 chr20: 43,674,346-43,675,972 , GRCh37.p13 chr20: 42,302,986-42,304,612 MYBL2
    nsv6550713copy number variation1nstd223human GRCh38 chr20: 43,674,467-43,680,640 , GRCh37.p13 chr20: 42,303,107-42,309,280 MYBL2
    nsv6544035copy number variation1nstd223human GRCh38 chr20: 43,658,386-43,665,921 , GRCh37.p13 chr20: 42,287,026-42,294,561 MYBL2
    nsv6542120copy number variation1nstd223human GRCh38 chr20: 43,690,101-43,697,000 , GRCh37.p13 chr20: 42,318,741-42,325,640 MYBL2
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