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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887494copy number variation1nstd209human GRCh38 chr1: 192,263,809-193,558,335 , GRCh37.p13 chr1: 192,232,939-193,527,465 , LINC01031, 22 more genes
    nsv5877280copy number variation1nstd209human GRCh38 chr1: 192,579,422-192,657,019 , GRCh37.p13 chr1: 192,548,552-192,626,149 RGS1, LOC105371664, 2 more genes
    nsv5828798copy number variation1nstd209human GRCh38 chr1: 192,519,315-192,609,010 , GRCh37.p13 chr1: 192,488,445-192,578,140 RGS1, LOC105371664, 1 more genes
    nsv5828486copy number variation2nstd209human GRCh38 chr1: 192,573,980-192,656,775 , GRCh37.p13 chr1: 192,543,110-192,625,905 LOC105371664, LOC107985241, 2 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4904169copy number variation1nstd200human GRCh38 chr1: 192,384,028-192,630,290 , GRCh37.p13 chr1: 192,353,158-192,599,420 RGS1, LOC105371664, 1 more genes
    nsv4904119copy number variation1nstd200human GRCh38 chr1: 187,280,074-192,928,506 , GRCh37.p13 chr1: 187,249,206-192,897,636 MIR4426, LINC01701, 40 more genes
    nsv4781323copy number variation1nstd200human GRCh37 chr1: 187,249,206-192,897,636 , GRCh38.p12 chr1: 187,280,074-192,928,506 LOC105371657, RPS27AP5, 40 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 QSOX1, PTPRC, 263 more genes
    nsv4594169copy number variation1nstd183human GRCh37 chr1: 192,574,005-192,582,712 , GRCh38.p12 chr1: 192,604,875-192,613,582 LOC107985241, LOC105371664
    nsv4535874insertion1nstd166human GRCh37.p13 chr1: 192,585,207-192,585,207 , GRCh38.p12 chr1: 192,616,077-192,616,077 LOC105371664, LOC107985241
    nsv4533675insertion1nstd166human GRCh37.p13 chr1: 192,585,186-192,585,186 , GRCh38.p12 chr1: 192,616,056-192,616,056 LOC107985241, LOC105371664
    nsv4532834insertion1nstd166human GRCh37.p13 chr1: 192,585,232-192,585,232 , GRCh38.p12 chr1: 192,616,102-192,616,102 LOC105371664, LOC107985241
    nsv4459804mobile element insertion1nstd166human GRCh37.p13 chr1: 192,602,447-192,602,447 , GRCh38.p12 chr1: 192,633,317-192,633,317 LOC107985241
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
    nsv4068335copy number variation1nstd166human GRCh37.p13 chr1: 192,601,282-192,685,589 , GRCh38.p12 chr1: 192,632,152-192,716,459 RGS13, LOC107985241, 2 more genes
    nsv4058055copy number variation1nstd166human GRCh37.p13 chr1: 192,599,006-192,613,069 , GRCh38.p12 chr1: 192,629,876-192,643,939 LOC107985241, RGS13
    nsv4053023copy number variation1nstd166human GRCh37.p13 chr1: 192,582,271-192,582,327 , GRCh38.p12 chr1: 192,613,141-192,613,197 LOC107985241, LOC105371664
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