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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885089copy number variation1nstd209human GRCh38 chr1: 111,414,892-111,414,960 , GRCh37.p13 chr1: 111,957,514-111,957,582 OVGP1
    nsv5880056copy number variation1nstd209human GRCh38 chr1: 111,195,040-111,530,461 , GRCh37.p13 chr1: 111,737,662-112,073,083 , PGBP, 17 more genes
    nsv5581184copy number variation1nstd207human GRCh38 chr1: 111,414,892-111,414,960 , GRCh37.p13 chr1: 111,957,514-111,957,582 OVGP1
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5353776translocation1nstd200human GRCh38 chr1: 111,424,827-111,424,827 , GRCh38 chr1: 111,424,774-111,424,774 , GRCh37.p13 chr1: 111,967,449-111,967,449 , GRCh37.p13 chr1: 111,967,396-111,967,396 OVGP1
    nsv5336135translocation1nstd200human GRCh37 chr1: 111,967,396-111,967,396 , GRCh37 chr1: 111,967,449-111,967,449 , GRCh38.p12 chr1: 111,424,827-111,424,827 , GRCh38.p12 chr1: 111,424,774-111,424,774 OVGP1
    nsv5075327mobile element insertion1nstd203human GRCh38 chr1: 111,423,065-111,423,081 , GRCh37.p13 chr1: 111,965,687-111,965,703 OVGP1
    nsv4890771copy number variation1nstd200human GRCh38 chr1: 111,422,465-111,429,717 , GRCh37.p13 chr1: 111,965,087-111,972,339 OVGP1
    nsv4890770copy number variation1nstd200human GRCh38 chr1: 111,409,791-111,416,259 , GRCh37.p13 chr1: 111,952,413-111,958,881 OVGP1
    nsv4773672copy number variation1nstd200human GRCh37 chr1: 111,965,087-111,972,339 , GRCh38.p12 chr1: 111,422,465-111,429,717 OVGP1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4738624copy number variation1nstd199human GRCh37 chr1: 111,957,506-111,957,575 , GRCh38.p12 chr1: 111,414,884-111,414,953 OVGP1
    nsv4593805copy number variation1nstd183human GRCh37 chr1: 111,857,216-112,148,517 , GRCh38.p12 chr1: 111,314,594-111,605,895 LOC105378904, HIGD1AP12, 14 more genes
    nsv4458728mobile element insertion1nstd166human GRCh37.p13 chr1: 111,956,562-111,956,562 , GRCh38.p12 chr1: 111,413,940-111,413,940 OVGP1
    nsv4454547copy number variation1nstd102humanPathogenic GRCh37 chr1: 110,994,179-112,360,446 , GRCh38.p12 chr1: 110,451,557-111,817,824 CCNT2P1, PROK1, 44 more genes
    nsv4439434copy number variation1nstd175human GRCh37 chr1: 111,957,514-111,957,583 , GRCh38.p12 chr1: 111,414,892-111,414,961 OVGP1
    nsv4405768copy number variation1nstd174human GRCh37 chr1: 111,957,191-111,957,907 , GRCh38.p12 chr1: 111,414,569-111,415,285 OVGP1
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