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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139766copy number variation1nstd232human GRCh37.p13 chr9: 134,391,120-134,391,174 , GRCh38.p12 chr9: 131,515,733-131,515,787 POMT1, LOC105376301
    nsv7098429copy number variation1nstd102humanUncertain significance GRCh37 chr9: 134,395,447-134,395,600 , GRCh38.p12 chr9: 131,520,060-131,520,213 POMT1
    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
    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
    nsv7076868inversion1nstd229human GRCh38 chr9: 131,266,802-131,706,679 , GRCh37.p13 chr9: 134,142,189-134,582,066 LOC105376301, PRRT1B, 10 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
    nsv7062185inversion1nstd229human GRCh38 chr9: 131,448,265-131,541,583 , GRCh37.p13 chr9: 134,323,652-134,416,970 UCK1, POMT1, 4 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
    nsv6875928copy number variation1nstd229human GRCh38 chr9: 131,487,035-131,704,810 , GRCh37.p13 chr9: 134,362,422-134,580,197 RAPGEF1, LOC105376301, 5 more genes
    nsv6870800copy number variation1nstd229human GRCh38 chr9: 131,517,106-131,517,183 , GRCh37.p13 chr9: 134,392,493-134,392,570 POMT1, LOC105376301
    nsv6869056copy number variation1nstd229human GRCh38 chr9: 131,228,357-131,624,747 , GRCh37.p13 chr9: 134,103,744-134,500,134 POMT1, UCK1, 11 more genes
    nsv6867232copy number variation1nstd229human GRCh38 chr9: 130,826,301-131,964,500 , GRCh37.p13 chr9: 133,701,688-134,839,887 SNORD62A, FAM78A, 21 more genes
    nsv6866237copy number variation1nstd229human GRCh38 chr9: 131,515,016-131,534,334 , GRCh37.p13 chr9: 134,390,403-134,409,721 POMT1, UCK1, 1 more genes
    nsv6864589copy number variation1nstd229human GRCh38 chr9: 131,302,727-131,623,767 , GRCh37.p13 chr9: 134,178,114-134,499,154 LOC105376299, SNORD62A, 9 more genes
    nsv6864386copy number variation1nstd229human GRCh38 chr9: 131,513,401-131,537,500 , GRCh37.p13 chr9: 134,388,788-134,412,887 UCK1, LOC105376301, 1 more genes
    nsv6859435copy number variation1nstd229human GRCh38 chr9: 131,220,301-131,964,500 , GRCh37.p13 chr9: 134,095,688-134,839,887 LOC105376300, NUP214, 14 more genes
    nsv6858605copy number variation1nstd229human GRCh38 chr9: 131,486,301-131,598,300 , GRCh37.p13 chr9: 134,361,688-134,473,687 UCK1, POMT1, 5 more genes
    nsv6636073copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 134,388,719-134,399,194 , GRCh38.p12 chr9: 131,513,332-131,523,807 POMT1, UCK1, 1 more genes
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