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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099198copy number variation1nstd231human GRCh38.p12 chr1: 44,129,375-46,768,878 , GRCh37 chr1: 44,595,047-47,234,550 PLK3, FAAH, 93 more genes
    nsv7095531copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,257,753-46,663,493 , GRCh38.p12 chr1: 43,792,082-46,197,821 AKR1A1, OSTCP5, 87 more genes
    nsv7055071inversion1nstd229human GRCh38 chr1: 43,970,005-47,371,780 , GRCh37.p13 chr1: 44,435,677-47,837,452 SNORD38A, PPIAP36, 121 more genes
    nsv7052236inversion1nstd229human GRCh38 chr1: 45,460,547-45,911,102 , GRCh37.p13 chr1: 45,926,219-46,376,774 MAST2, RPS15AP10, 16 more genes
    nsv6650728copy number variation1nstd229human GRCh38 chr1: 45,617,950-45,640,704 , GRCh37.p13 chr1: 46,083,622-46,106,376 GPBP1L1, CCDC17, 1 more genes
    nsv6650727copy number variation1nstd229human GRCh38 chr1: 45,595,150-45,595,189 , GRCh37.p13 chr1: 46,060,822-46,060,861 NASP
    nsv6650642copy number variation1nstd229human GRCh38 chr1: 45,607,168-45,675,189 , GRCh37.p13 chr1: 46,072,840-46,140,861 NASP, GPBP1L1, 3 more genes
    nsv6650511copy number variation1nstd229human GRCh38 chr1: 45,617,230-45,634,837 , GRCh37.p13 chr1: 46,082,902-46,100,509 GPBP1L1, CCDC17, 1 more genes
    nsv6650501copy number variation1nstd229human GRCh38 chr1: 45,347,008-45,611,537 , GRCh37.p13 chr1: 45,812,680-46,077,209 PRDX1, AKR1A1, 6 more genes
    nsv6650414copy number variation1nstd229human GRCh38 chr1: 45,466,152-45,640,828 , GRCh37.p13 chr1: 45,931,824-46,106,500 CCDC163, NASP, 7 more genes
    nsv6649986copy number variation1nstd229human GRCh38 chr1: 45,601,823-45,674,673 , GRCh37.p13 chr1: 46,067,495-46,140,345 CCDC17, RPL7AP16, 3 more genes
    nsv6649985copy number variation1nstd229human GRCh38 chr1: 45,591,866-45,669,654 , GRCh37.p13 chr1: 46,057,538-46,135,326 GPBP1L1, RPS15AP10, 3 more genes
    nsv6649978copy number variation1nstd229human GRCh38 chr1: 45,284,916-45,996,554 , GRCh37.p13 chr1: 45,750,588-46,462,226 HPDL, PPIAP36, 22 more genes
    nsv6544620inversion1nstd223human GRCh38 chr1: 45,592,283-45,593,251 , GRCh37.p13 chr1: 46,057,955-46,058,923 NASP
    nsv6332914copy number variation1nstd223human GRCh38 chr1: 45,619,012-45,624,753 , GRCh37.p13 chr1: 46,084,684-46,090,425 NASP, CCDC17
    nsv6320196copy number variation1nstd223human GRCh38 chr1: 45,605,219-45,606,432 , GRCh37.p13 chr1: 46,070,891-46,072,104 NASP
    nsv6316530copy number variation1nstd223human GRCh38 chr1: 45,617,230-45,634,837 , GRCh37.p13 chr1: 46,082,902-46,100,509 GPBP1L1, CCDC17, 1 more genes
    nsv6314936copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,346,001-46,332,161 , GRCh38.p12 chr1: 43,880,329-45,866,489 ZSWIM5, OSTCP5, 79 more genes
    nsv6313850copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,083,531-46,738,006 , GRCh38.p12 chr1: 45,617,859-46,272,334 LOC105378694, POMGNT1, 18 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
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