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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
    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
    nsv6877216copy number variation1nstd229human GRCh38 chr9: 133,211,147-133,214,380 , GRCh37.p13 chr9: 136,086,534-136,089,767 , GRCh37.p13 chr9|NW_003315925.1: 37,093-40,326 OBP2B
    nsv6867948copy number variation1nstd229human GRCh38 chr9: 133,206,018-133,206,082 , GRCh37.p13 chr9|NW_003315925.1: 31,964-32,028 , GRCh37.p13 chr9: 136,081,405-136,081,469 OBP2B
    nsv6633586copy number variation1nstd224human GRCh37 chr9: 136,031,412-136,173,565 , GRCh38.p12 chr9: 133,156,025-133,297,990 , GRCh38.p12 chr9|NW_009646201.1: 1-124,084 ABO, OBP2B, 2 more genes
    nsv6566738inversion1nstd223human GRCh37.p13 chr9|NW_003315925.1: 30,610-143,512 , GRCh38 chr9: 133,204,664-133,317,418 , GRCh37.p13 chr9: 136,080,051-136,184,253 ABO, OBP2B, 2 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
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6308706insertion1nstd186human GRCh37 chr9: 136,097,437-136,097,487 , GRCh38.p12 chr9: 133,222,050-133,222,100 , GRCh38.p12 chr9|NW_009646201.1: 47,996-48,046 OBP2B
    nsv6308071mobile element insertion1nstd186human GRCh37 chr9: 136,093,537-136,093,575 , GRCh38.p12 chr9: 133,218,150-133,218,188 , GRCh38.p12 chr9|NW_009646201.1: 44,096-44,134 OBP2B
    nsv6268862copy number variation1nstd214human GRCh38 chr9: 133,223,553-133,223,624 , GRCh37.p13 chr9|NW_003315925.1: 49,499-49,570 , GRCh37.p13 chr9: 136,098,940-136,099,011 OBP2B, LCN1P1
    nsv6268765copy number variation1nstd214human GRCh38 chr9: 133,206,018-133,206,081 , GRCh37.p13 chr9|NW_003315925.1: 31,964-32,027 , GRCh37.p13 chr9: 136,081,405-136,081,468 OBP2B
    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
    nsv6094273insertion1nstd212human GRCh38 chr9: 133,222,140-133,222,140 , GRCh37.p13 chr9|NW_003315925.1: 48,086-48,086 , GRCh37.p13 chr9: 136,097,527-136,097,527 OBP2B
    nsv6014912copy number variation1nstd212human GRCh38 chr9: 133,206,020-133,206,084 , GRCh37.p13 chr9: 136,081,407-136,081,471 , GRCh37.p13 chr9|NW_003315925.1: 31,966-32,030 OBP2B
    nsv5974643inversion1nstd209human GRCh38 chr9: 133,204,664-133,317,417 , GRCh37.p13 chr9: 136,080,051-136,184,252 , GRCh37.p13 chr9|NW_003315925.1: 30,610-143,511 ABO, OBP2B, 2 more genes
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