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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142890insertion1nstd232human GRCh37.p13 chr9: 136,905,394-136,905,394 , GRCh38.p12 chr9: 134,040,272-134,040,272 BRD3
    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
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 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
    nsv7060209inversion1nstd229human GRCh38 chr9: 133,220,670-135,537,297 , GRCh37.p13 chr9: 136,369,193-138,429,143 COL5A1, DBH, 66 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
    nsv6889955copy number variation1nstd229human GRCh38 chr9: 133,985,801-134,102,600 , GRCh37.p13 chr9: 136,850,923-136,967,722 LOC100130548, VAV2, 3 more genes
    nsv6888178copy number variation1nstd229human GRCh38 chr9: 134,026,732-134,055,452 , GRCh37.p13 chr9: 136,891,854-136,920,574 BRD3OS, LOC100130548, 1 more genes
    nsv6886856copy number variation1nstd229human GRCh38 chr9: 134,033,852-134,033,891 , GRCh37.p13 chr9: 136,898,974-136,899,013 BRD3
    nsv6883877copy number variation1nstd229human GRCh38 chr9: 134,041,821-134,043,549 , GRCh37.p13 chr9: 136,906,943-136,908,671 BRD3
    nsv6880465copy number variation1nstd229human GRCh38 chr9: 134,051,240-134,051,410 , GRCh37.p13 chr9: 136,916,362-136,916,532 BRD3
    nsv6878255copy number variation1nstd229human GRCh38 chr9: 133,857,124-134,045,081 , GRCh37.p13 chr9: 136,722,246-136,910,203 BRD3, VAV2, 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
    nsv6435681copy number variation1nstd223human GRCh38 chr9: 133,857,124-134,045,081 , GRCh37.p13 chr9: 136,722,246-136,910,203 BRD3, BRD3OS, 1 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
    nsv6300786copy number variation1nstd186human GRCh37 chr9: 136,920,682-136,921,884 , GRCh38.p12 chr9: 134,055,560-134,056,762 LOC100130548, BRD3
    nsv6137060copy number variation1nstd213human GRCh37 chr9: 135,710,000-137,020,001 , GRCh38.p12 chr9: 132,834,613-134,154,879 CELP, SURF1, 47 more genes
    nsv5916843copy number variation1nstd209human GRCh38 chr9: 134,026,732-134,055,450 , GRCh37.p13 chr9: 136,891,854-136,920,572 LOC100130548, BRD3OS, 1 more genes
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