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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6874300copy number variation1nstd229human GRCh38 chr9: 128,129,337-128,131,861 , GRCh37.p13 chr9: 130,891,616-130,894,140 PTGES2-AS1
    nsv6871648copy number variation1nstd229human GRCh38 chr9: 128,121,320-128,126,662 , GRCh37.p13 chr9: 130,883,599-130,888,941 PTGES2-AS1, PTGES2
    nsv6858409copy number variation1nstd229human GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979 BBLN, SH2D3C, 47 more genes
    nsv6858157copy number variation1nstd229human GRCh38 chr9: 128,079,047-128,161,482 , GRCh37.p13 chr9: 130,841,326-130,923,761 BBLN, PTGES2, 4 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
    nsv6445830copy number variation1nstd223human GRCh38 chr9: 127,317,501-128,138,900 , GRCh37.p13 chr9: 130,079,780-130,901,179 STXBP1, PTGES2-AS1, 34 more genes
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 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
    nsv6312681copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857 EEIG1, PIP5KL1, 32 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6000760copy number variation1nstd212human GRCh38 chr9: 128,129,949-128,130,316 , GRCh37.p13 chr9: 130,892,228-130,892,595 PTGES2-AS1
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv4985740copy number variation1nstd200human GRCh38 chr9: 128,105,845-128,709,294 , GRCh37.p13 chr9: 130,868,124-131,471,573 , SET, 33 more genes
    nsv4985738copy number variation1nstd200human GRCh38 chr9: 128,030,482-128,145,703 , GRCh37.p13 chr9: 130,792,761-130,907,982 SLC25A25-AS1, NAIF1, 3 more genes
    nsv4983736copy number variation1nstd200human GRCh38 chr9: 128,128,168-128,132,401 , GRCh37.p13 chr9: 130,890,447-130,894,680 PTGES2-AS1, PTGES2
    nsv4768374copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685 COQ4, GLE1, 53 more genes
    nsv4714076copy number variation1nstd195human GRCh37 chr9: 130,892,801-130,900,651 , GRCh38.p12 chr9: 128,130,522-128,138,372 PTGES2-AS1
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