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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137071copy number variation1nstd102humannot provided GRCh37 chr1: 72,536,773-72,771,521 , GRCh38.p12 chr1: 72,071,090-72,305,838 GDI2P2, LOC105378797, 2 more genes
    nsv7099298copy number variation1nstd231human GRCh38.p12 chr1: 68,115,402-81,183,740 , GRCh37 chr1: 68,581,085-81,649,425 ACADM, COX6A1P1, 145 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv6654104copy number variation1nstd229human GRCh38 chr1: 72,300,641-72,346,158 , GRCh37.p13 chr1: 72,766,324-72,811,841 LOC105378797, RPL31P12
    nsv6653564copy number variation1nstd229human GRCh38 chr1: 72,151,012-72,368,493 , GRCh37.p13 chr1: 72,616,695-72,834,176 GDI2P2, NEGR1, 2 more genes
    nsv6332241copy number variation1nstd223human GRCh38 chr1: 72,280,801-72,305,300 , GRCh37.p13 chr1: 72,746,484-72,770,983 NEGR1, LOC105378797, 1 more genes
    nsv6329313copy number variation1nstd223human GRCh38 chr1: 72,164,596-72,682,639 , GRCh37.p13 chr1: 72,630,279-73,148,322 GDI2P2, RPL31P12, 3 more genes
    nsv6327857copy number variation1nstd223human GRCh38 chr1: 72,290,001-72,370,200 , GRCh37.p13 chr1: 72,755,684-72,835,883 LOC105378797, RPL31P12
    nsv6319322copy number variation1nstd223human GRCh38 chr1: 72,290,201-72,368,500 , GRCh37.p13 chr1: 72,755,884-72,834,183 RPL31P12, LOC105378797
    nsv6315306copy number variation1nstd102humanUncertain significance GRCh38 chr1: 66,885,559-77,949,895 , GRCh37.p13 chr1: 67,351,242-78,415,580 DNAJB6P4, LRRC7, 137 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6133720copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,840 , GRCh38.p12 chr1: 72,300,641-72,346,157 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,382 RPL31P12, LOC105378797
    nsv6133719copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,840 , GRCh38.p12 chr1: 72,300,641-72,346,157 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,382 RPL31P12, LOC105378797
    nsv6133541copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,838 , GRCh38.p12 chr1: 72,300,641-72,346,155 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,380 RPL31P12, LOC105378797
    nsv6133540copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,839 , GRCh38.p12 chr1: 72,300,641-72,346,156 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,381 RPL31P12, LOC105378797
    nsv6133539copy number variation1nstd213human GRCh37 chr1: 72,766,281-72,811,840 , GRCh38.p12 chr1: 72,300,598-72,346,157 , GRCh38.p12 chr1|NW_018654707.1: 12,865-67,382 RPL31P12, LOC105378797
    nsv6133489copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,871 , GRCh38.p12 chr1: 72,300,641-72,346,188 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,413 RPL31P12, LOC105378797
    nsv6133488copy number variation2nstd213human GRCh37 chr1: 72,766,324-72,811,840 , GRCh38.p12 chr1: 72,300,641-72,346,157 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,382 RPL31P12, LOC105378797
    nsv6133420copy number variation1nstd213human GRCh37 chr1: 72,766,324-72,811,836 , GRCh38.p12 chr1: 72,300,641-72,346,153 , GRCh38.p12 chr1|NW_018654707.1: 12,908-67,378 RPL31P12, LOC105378797
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