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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077300inversion1nstd229human GRCh38 chr20: 52,706,618-56,026,754 , GRCh37.p13 chr20: 51,323,157-54,601,810 TSHZ2, LOC105372671, 26 more genes
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7072131inversion1nstd229human GRCh38 chr20: 53,548,074-57,294,874 , GRCh37.p13 chr20: 52,164,613-55,869,930 CBLN4, RNU6-1146P, 46 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7068894inversion1nstd229human GRCh38 chr20: 53,603,613-53,614,724 , GRCh37.p13 chr20: 52,220,152-52,231,263 LOC105372672, ZNF217
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7063790inversion1nstd229human GRCh38 chr20: 53,606,224-53,609,205 , GRCh37.p13 chr20: 52,222,763-52,225,744 ZNF217, LOC105372672
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058989inversion1nstd229human GRCh38 chr20: 52,927,440-57,459,107 , GRCh37.p13 chr20: 51,543,979-56,034,163 FAM210B, RPS4XP3, 61 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7058201inversion1nstd229human GRCh38 chr20: 51,845,371-57,066,404 , GRCh37.p13 chr20: 50,461,910-55,641,460 RNU6-347P, RPS4XP3, 61 more genes
    nsv7037792copy number variation1nstd229human GRCh38 chr20: 53,628,751-53,630,311 , GRCh37.p13 chr20: 52,245,290-52,246,850 LOC105372672
    nsv7037347copy number variation1nstd229human GRCh38 chr20: 53,493,901-53,825,400 , GRCh37.p13 chr20: 52,110,440-52,441,939 LOC105372672, RNU7-14P, 4 more genes
    nsv7035032copy number variation1nstd229human GRCh38 chr20: 53,628,698-53,630,410 , GRCh37.p13 chr20: 52,245,237-52,246,949 LOC105372672
    nsv7033153copy number variation1nstd229human GRCh38 chr20: 53,601,781-53,607,702 , GRCh37.p13 chr20: 52,218,320-52,224,241 ZNF217, LOC105372672
    nsv7027386copy number variation1nstd229human GRCh38 chr20: 53,608,901-53,614,400 , GRCh37.p13 chr20: 52,225,440-52,230,939 ZNF217, LOC105372672
    nsv7025139copy number variation1nstd229human GRCh38 chr20: 53,628,101-53,630,400 , GRCh37.p13 chr20: 52,244,640-52,246,939 LOC105372672
    nsv7019920copy number variation1nstd229human GRCh38 chr20: 53,617,288-53,631,171 , GRCh37.p13 chr20: 52,233,827-52,247,710 LOC105372672
    nsv7019135copy number variation1nstd229human GRCh38 chr20: 53,626,393-53,626,427 , GRCh37.p13 chr20: 52,242,932-52,242,966 LOC105372672
    nsv6599481inversion1nstd223human GRCh38 chr20: 53,619,310-53,620,351 , GRCh37.p13 chr20: 52,235,849-52,236,890 LOC105372672
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