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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098431copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,775,735-135,866,437 , GRCh38.p12 chr9: 132,900,348-132,991,050 RPL39P24, TSC1, 3 more genes
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097935copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,820,391-135,821,434 , GRCh38.p12 chr9: 132,945,004-132,946,047 TSC1, GFI1B, 1 more genes
    nsv7097932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,884,602-135,942,612 , GRCh38.p12 chr9: 131,009,215-133,067,225 LAMC3, SPACA9, 40 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6870495copy number variation1nstd229human GRCh38 chr9: 132,968,722-132,968,891 , GRCh37.p13 chr9: 135,844,109-135,844,278 GFI1B
    nsv6870007copy number variation1nstd229human GRCh38 chr9: 132,916,912-133,049,166 , GRCh37.p13 chr9: 135,792,299-135,924,553 SNORD141A, MIR548AW, 7 more genes
    nsv6866176copy number variation1nstd229human GRCh38 chr9: 132,944,966-132,950,750 , GRCh37.p13 chr9: 135,820,353-135,826,137 TSC1, GFI1B, 1 more genes
    nsv6865986copy number variation1nstd229human GRCh38 chr9: 132,978,377-132,982,363 , GRCh37.p13 chr9: 135,853,764-135,857,750 GFI1B
    nsv6862894copy number variation1nstd229human GRCh38 chr9: 132,986,276-132,986,330 , GRCh37.p13 chr9: 135,861,663-135,861,717 GFI1B
    nsv6637649copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,354,006-135,950,908 , GRCh38.p12 chr9: 132,478,619-133,075,521 GFI1B, SNORD141A, 15 more genes
    nsv6560740inversion1nstd223human GRCh38 chr9: 132,962,217-132,963,080 , GRCh37.p13 chr9: 135,837,604-135,838,467 GFI1B, RNU7-21P, 1 more genes
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6447065copy number variation1nstd223human GRCh38 chr9: 132,969,481-132,971,327 , GRCh37.p13 chr9: 135,844,868-135,846,714 GFI1B
    nsv6444987copy number variation1nstd223human GRCh38 chr9: 132,916,912-133,049,166 , GRCh37.p13 chr9: 135,792,299-135,924,553 GTF3C5, MIR548AW, 7 more genes
    nsv6437479copy number variation1nstd223human GRCh38 chr9: 132,991,301-132,993,400 , GRCh37.p13 chr9: 135,866,688-135,868,787 GFI1B
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