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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147664copy number variation1nstd232human GRCh37.p13 chr1: 182,710,450-182,710,498 , GRCh38.p12 chr1: 182,741,315-182,741,363 RGS8
    nsv7099254copy number variation1nstd231human GRCh38.p12 chr1: 182,376,401-191,898,122 , GRCh37 chr1: 182,345,536-191,867,252 DHX9, GLUL, 99 more genes
    nsv6646034copy number variation1nstd229human GRCh38 chr1: 182,734,173-182,846,522 , GRCh37.p13 chr1: 182,703,308-182,815,657 LOC100421471, DHX9-AS1, 3 more genes
    nsv6646033copy number variation1nstd229human GRCh38 chr1: 182,704,875-182,708,654 , GRCh37.p13 chr1: 182,674,010-182,677,789 RGS8
    nsv6645971copy number variation1nstd229human GRCh38 chr1: 182,694,501-182,697,200 , GRCh37.p13 chr1: 182,663,636-182,666,335 RGS8
    nsv6645899copy number variation1nstd229human GRCh38 chr1: 182,666,601-182,689,500 , GRCh37.p13 chr1: 182,635,736-182,658,635 RGS8
    nsv6645898copy number variation1nstd229human GRCh38 chr1: 182,653,434-182,653,567 , GRCh37.p13 chr1: 182,622,569-182,622,702 RGS8
    nsv6645522copy number variation1nstd229human GRCh38 chr1: 182,705,545-182,705,725 , GRCh37.p13 chr1: 182,674,680-182,674,860 RGS8
    nsv6645521copy number variation1nstd229human GRCh38 chr1: 182,650,041-182,650,174 , GRCh37.p13 chr1: 182,619,176-182,619,309 RGS8
    nsv6645520copy number variation1nstd229human GRCh38 chr1: 182,617,084-182,652,951 , GRCh37.p13 chr1: 182,586,219-182,622,086 LINC01686, RGS8
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    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
    nsv6636857copy number variation1nstd102humanUncertain significance GRCh37 chr1: 182,442,865-182,609,349 , GRCh38.p12 chr1: 182,473,730-182,640,214 RGSL1, RGS16, 3 more genes
    nsv6636465copy number variation1nstd102humanUncertain significance GRCh37 chr1: 182,443,031-182,609,230 , GRCh38.p12 chr1: 182,473,896-182,640,095 LINC01686, RGSL1, 3 more genes
    nsv6625927copy number variation1nstd224human GRCh37 chr1: 182,449,249-182,611,109 , GRCh38.p12 chr1: 182,480,114-182,641,974 RNASEL, RGS16, 3 more genes
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6332661copy number variation1nstd223human GRCh38 chr1: 182,716,061-182,716,400 , GRCh37.p13 chr1: 182,685,196-182,685,535 RGS8
    nsv6332283copy number variation1nstd223human GRCh38 chr1: 182,647,607-182,648,260 , GRCh37.p13 chr1: 182,616,742-182,617,395 RGS8
    nsv6328929copy number variation1nstd223human GRCh38 chr1: 182,730,499-182,730,907 , GRCh37.p13 chr1: 182,699,634-182,700,042 RGS8
    nsv6326585copy number variation1nstd223human GRCh38 chr1: 182,705,544-182,705,725 , GRCh37.p13 chr1: 182,674,679-182,674,860 RGS8
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