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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148151copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,486,532-37,745,203 , GRCh37.p13 chr17: 34,900,240-35,888,667 PIGW, LOC105371751, 32 more genes
    nsv7148119copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,752,221-36,105,007 , GRCh38.p12 chr17|NT_187614.1: 694,163-1,984,072 , GRCh38.p12 chr17: 36,446,545-37,745,016 LOC105371756, SYNRG, 35 more genes
    nsv7144359copy number variation1nstd232human GRCh37.p13 chr17: 34,942,394-34,942,477 , GRCh38.p12 chr17: 36,585,964-36,586,047 , GRCh38.p12 chr17|NT_187614.1: 821,459-821,542 GGNBP2
    nsv7137104copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,545-36,293,050 , GRCh38.p12 chr17: 36,486,701-37,933,506 , GRCh38.p12 chr17|NT_187614.1: 721,605-2,172,115 LHX1-DT, LOC105371749, 40 more genes
    nsv7098907copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,138,501-37,924,067 , GRCh37.p13 chr17: 34,900,240-35,888,667 LOC102723414, SYNRG, 51 more genes
    nsv7098735copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 34,842,542-36,104,877 , GRCh38.p12 chr17: 36,486,698-37,744,886 , GRCh38.p12 chr17|NT_187614.1: 721,602-1,983,942 ACACA, LHX1, 34 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7070483inversion1nstd229human GRCh38 chr17: 36,507,875-36,562,214 , GRCh37.p13 chr17|NW_003315949.1: 392,625-429,138 GGNBP2, MYO19, 1 more genes
    nsv6997003copy number variation1nstd229human GRCh38 chr17: 36,562,684-36,567,633 , GRCh37.p13 chr17: 34,918,524-34,921,981 GGNBP2
    nsv6990638copy number variation1nstd229human GRCh38 chr17: 36,555,286-36,555,917 , GRCh37.p13 chr17: 34,911,127-34,911,758 GGNBP2
    nsv6984191copy number variation1nstd229human GRCh38 chr17: 36,570,989-36,572,020 , GRCh37.p13 chr17: 34,926,828-34,927,859 GGNBP2
    nsv6981293copy number variation1nstd229human GRCh38 chr17: 36,587,794-36,715,996 , GRCh37.p13 chr17: 34,944,224-35,072,312 LOC107985031, MRM1, 4 more genes
    nsv6637369copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,425,363-36,404,555 , GRCh38.p12 chr17|NT_187614.1: 332,891-2,283,620 CCL3L3, MRM1, 63 more genes
    nsv6634438copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,842,544-36,104,875 , GRCh38.p12 chr17: 36,486,700-37,744,884 , GRCh38.p12 chr17|NT_187614.1: 721,604-1,983,940 HNF1B, LOC100419621, 34 more genes
    nsv6634420copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,822,465-36,243,781 , GRCh38.p12 chr17|NT_187614.1: 701,523-2,122,846 , GRCh38.p12 chr17: 36,466,619-37,884,161 GGNBP2, AATF, 36 more genes
    nsv6624272copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,249,430 , GRCh38.p12 chr17: 36,459,737-37,889,808 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,128,495 DDX52, DUSP14, 36 more genes
    nsv6623850copy number variation1nstd224human GRCh37 chr17: 34,815,551-36,411,684 , GRCh38.p12 chr17|NT_187614.1: 694,641-2,290,749 LHX1, HNF1B, 44 more genes
    nsv6595427inversion1nstd223human GRCh38 chr17: 36,587,687-36,588,407 , GRCh37.p13 chr17: 34,944,117-34,944,837 GGNBP2
    nsv6594577inversion1nstd223human GRCh38 chr17: 36,548,616-36,549,234 , GRCh37.p13 chr17: 34,904,465-34,905,075 GGNBP2
    nsv6588992inversion1nstd223human GRCh38 chr17: 36,581,223-36,581,598 , GRCh37.p13 chr17: 34,937,653-34,938,028 GGNBP2
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