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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6893734copy number variation1nstd229human GRCh38 chr9: 133,514,100-133,514,430 , GRCh37.p13 chr9: 136,379,222-136,379,552 MYMK
    nsv6890493copy number variation1nstd229human GRCh38 chr9: 133,512,888-133,513,629 , GRCh37.p13 chr9: 136,378,010-136,378,751 MYMK
    nsv6882097copy number variation1nstd229human GRCh38 chr9: 133,509,988-133,513,350 , GRCh37.p13 chr9: 136,375,110-136,378,472 MYMK
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6455467copy number variation1nstd223human GRCh38 chr9: 133,514,088-133,514,430 , GRCh37.p13 chr9: 136,379,210-136,379,552 MYMK
    nsv6450146copy number variation1nstd223human GRCh38 chr9: 133,511,608-133,514,768 , GRCh37.p13 chr9: 136,376,730-136,379,890 MYMK
    nsv6445025copy number variation1nstd223human GRCh38 chr9: 133,518,523-133,518,925 , GRCh37.p13 chr9: 136,383,645-136,384,047 MYMK
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    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
    nsv6020061copy number variation1nstd212human GRCh38 chr9: 133,514,088-133,514,430 , GRCh37.p13 chr9: 136,379,210-136,379,552 MYMK
    nsv5917634copy number variation1nstd209human GRCh38 chr9: 133,514,088-133,514,429 , GRCh37.p13 chr9: 136,379,210-136,379,551 MYMK
    nsv5595395copy number variation1nstd207human GRCh38 chr9: 133,514,088-133,514,429 , GRCh37.p13 chr9: 136,379,210-136,379,551 MYMK
    nsv5489828copy number variation1nstd206human GRCh38 chr9: 133,514,100-133,514,430 , GRCh37.p13 chr9: 136,379,222-136,379,552 MYMK
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