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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098049copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,037,910-116,993,432 , GRCh38.p12 chr9: 113,275,630-114,231,152 POLE3, LOC100132609, 20 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6562917inversion1nstd223human GRCh38 chr9: 113,394,012-113,394,425 , GRCh37.p13 chr9: 116,156,292-116,156,705 ALAD
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313987copy number variation1nstd102humanUncertain significance GRCh37 chr9: 115,883,313-116,179,965 , GRCh38.p12 chr9: 113,121,033-113,417,685 HDHD3, BSPRY, 11 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312747copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,041,205-116,155,839 , GRCh38.p12 chr9: 113,278,925-113,393,559 HDHD3, RNF183, 4 more genes
    nsv6136360copy number variation1nstd213human GRCh37 chr9: 116,050,000-116,700,001 , GRCh38.p12 chr9: 113,287,720-113,937,721 RGS3, C9orf43, 13 more genes
    nsv6136359copy number variation1nstd213human GRCh37 chr9: 116,050,000-116,290,001 , GRCh38.p12 chr9: 113,287,720-113,527,721 ALAD, RGS3, 7 more genes
    nsv6136358copy number variation1nstd213human GRCh37 chr9: 115,820,000-116,410,001 , GRCh38.p12 chr9: 113,057,720-113,647,721 RGS3, PRPF4, 16 more genes
    nsv5924836copy number variation1nstd209human GRCh38 chr9: 113,395,802-113,398,525 , GRCh37.p13 chr9: 116,158,082-116,160,805 ALAD
    nsv5917074copy number variation1nstd209human GRCh38 chr9: 113,384,381-113,385,400 , GRCh37.p13 chr9: 116,146,661-116,147,680 ALAD
    nsv5864391copy number variation1nstd209human GRCh38 chr9: 113,384,324-113,385,423 , GRCh37.p13 chr9: 116,146,604-116,147,703 ALAD
    nsv5859774copy number variation1nstd209human GRCh38 chr9: 113,396,282-113,398,781 , GRCh37.p13 chr9: 116,158,562-116,161,061 ALAD
    nsv5319083copy number variation1nstd204human GRCh37.p13 chr9: 116,077,135-116,147,801 , GRCh38.p13 chr9: 113,314,855-113,385,521 ALAD, BSPRY, 2 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4830371copy number variation1nstd200human GRCh37 chr9: 116,077,143-116,147,794 , GRCh38.p12 chr9: 113,314,863-113,385,514 BSPRY, WDR31, 2 more genes
    nsv4568935mobile element insertion1nstd166human GRCh37.p13 chr9: 116,163,925-116,163,925 , GRCh38.p12 chr9: 113,401,645-113,401,645 ALAD
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