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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144266copy number variation1nstd232human GRCh37.p13 chr1: 192,609,798-192,609,863 , GRCh38.p12 chr1: 192,640,668-192,640,733 RGS13
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7057871inversion1nstd229human GRCh38 chr1: 191,728,426-196,575,913 , GRCh37.p13 chr1: 191,697,556-196,545,043 GLRX2, LOC107985241, 37 more genes
    nsv7044147inversion1nstd229human GRCh38 chr1: 190,518,287-195,020,156 , GRCh37.p13 chr1: 190,487,417-194,989,286 LOC105371668, B3GALT2, 34 more genes
    nsv7040010inversion1nstd229human GRCh38 chr1: 192,605,635-192,676,399 , GRCh37.p13 chr1: 192,574,765-192,645,529 RGS13, LOC107985241, 1 more genes
    nsv6676784copy number variation1nstd229human GRCh38 chr1: 192,648,763-192,661,498 , GRCh37.p13 chr1: 192,617,893-192,630,628 RGS13
    nsv6676266copy number variation1nstd229human GRCh38 chr1: 192,640,668-192,640,734 , GRCh37.p13 chr1: 192,609,798-192,609,864 RGS13
    nsv6674294copy number variation1nstd229human GRCh38 chr1: 192,652,028-192,654,241 , GRCh37.p13 chr1: 192,621,158-192,623,371 RGS13
    nsv6672055copy number variation1nstd229human GRCh38 chr1: 192,651,101-192,667,500 , GRCh37.p13 chr1: 192,620,231-192,636,630 RGS13
    nsv6667258copy number variation1nstd229human GRCh38 chr1: 192,506,401-192,720,100 , GRCh37.p13 chr1: 192,475,531-192,689,230 RGS13, LOC107985241, 4 more genes
    nsv6667188copy number variation1nstd229human GRCh38 chr1: 192,660,401-192,671,700 , GRCh37.p13 chr1: 192,629,531-192,640,830 RGS13
    nsv6666223copy number variation1nstd229human GRCh38 chr1: 192,625,150-192,706,244 , GRCh37.p13 chr1: 192,594,280-192,675,374 RGS13, LOC105371664, 1 more genes
    nsv6665374copy number variation1nstd229human GRCh38 chr1: 192,506,601-192,661,100 , GRCh37.p13 chr1: 192,475,731-192,630,230 LOC107985241, RGS1, 2 more genes
    nsv6664098copy number variation1nstd229human GRCh38 chr1: 189,813,413-194,218,341 , GRCh37.p13 chr1: 189,782,543-194,187,471 RO60, MIR4426, 38 more genes
    nsv6662173copy number variation1nstd229human GRCh38 chr1: 192,630,001-192,779,900 , GRCh37.p13 chr1: 192,599,131-192,749,030 RGS13, RPS27AP5, 3 more genes
    nsv6658734copy number variation1nstd229human GRCh38 chr1: 192,632,152-192,716,463 , GRCh37.p13 chr1: 192,601,282-192,685,593 MIR4426, LOC107985241, 2 more genes
    nsv6658214copy number variation1nstd229human GRCh38 chr1: 192,660,601-192,698,300 , GRCh37.p13 chr1: 192,629,731-192,667,430 RGS13
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6636659copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 189,633,885-199,854,163 , GRCh38.p12 chr1: 189,664,755-199,885,035 F13B, CFH, 88 more genes
    nsv6541970inversion1nstd223human GRCh38 chr1: 192,642,954-192,643,869 , GRCh37.p13 chr1: 192,612,084-192,612,999 RGS13
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