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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143218insertion1nstd232human GRCh37.p13 chr9: 136,258,359-136,258,359 , GRCh38.p12 chr9: 133,392,583-133,392,583 , GRCh38.p12 chr9|NW_009646201.1: 218,677-218,677 STKLD1
    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
    nsv6895332copy number variation1nstd229human GRCh38 chr9: 133,389,210-133,394,833 , GRCh37.p13 chr9: 136,254,994-136,259,960 , GRCh37.p13 chr9|NW_003315925.1: 215,304-220,927 STKLD1
    nsv6892307copy number variation1nstd229human GRCh38 chr9: 133,395,720-133,395,887 , GRCh37.p13 chr9: 136,260,847-136,261,014 , GRCh37.p13 chr9|NW_003315925.1: 221,814-221,981 STKLD1
    nsv6890123copy number variation1nstd229human GRCh38 chr9: 133,388,956-133,400,474 , GRCh37.p13 chr9|NW_003315925.1: 215,050-226,568 , GRCh37.p13 chr9: 136,254,740-136,265,602 STKLD1
    nsv6889063copy number variation1nstd229human GRCh38 chr9: 133,382,154-133,389,508 , GRCh37.p13 chr9: 136,249,026-136,255,292 , GRCh37.p13 chr9|NW_003315925.1: 208,248-215,602 STKLD1
    nsv6884853copy number variation1nstd229human GRCh38 chr9: 133,316,801-133,500,200 , GRCh37.p13 chr9|NW_003315925.1: 142,895-326,294 , GRCh37.p13 chr9: 136,183,638-136,365,322 SURF2, SURF6, 16 more genes
    nsv6884782copy number variation1nstd229human GRCh38 chr9: 133,391,126-133,391,176 , GRCh37.p13 chr9|NW_003315925.1: 217,220-217,270 , GRCh37.p13 chr9: 136,256,902-136,256,952 STKLD1
    nsv6883190copy number variation1nstd229human GRCh38 chr9: 133,393,667-133,397,301 , GRCh37.p13 chr9|NW_003315925.1: 219,761-223,395 , GRCh37.p13 chr9: 136,258,794-136,262,428 STKLD1
    nsv6882057copy number variation1nstd229human GRCh38 chr9: 133,316,601-133,495,400 , GRCh37.p13 chr9|NW_003315925.1: 142,695-321,494 , GRCh37.p13 chr9: 136,183,438-136,360,522 LCN1P2, SURF4, 16 more genes
    nsv6878543copy number variation1nstd229human GRCh38 chr9: 133,398,902-133,401,329 , GRCh37.p13 chr9: 136,264,031-136,266,458 , GRCh37.p13 chr9|NW_003315925.1: 224,996-227,423 STKLD1
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6455565copy number variation1nstd223human GRCh38 chr9: 133,398,533-133,445,103 , GRCh37.p13 chr9: 136,263,660-136,310,224 , GRCh37.p13 chr9|NW_003315925.1: 224,627-271,197 REXO4, STKLD1, 1 more genes
    nsv6454855copy number variation1nstd223human GRCh38 chr9: 133,383,145-133,383,829 , GRCh37.p13 chr9|NW_003315925.1: 209,239-209,923 STKLD1
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