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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917804copy number variation1nstd209human GRCh38 chr9: 68,467,657-68,468,767 , GRCh37.p13 chr9|NW_003871067.1: 247,105-248,215 , GRCh37.p13 chr9: 71,082,573-71,083,683 PGM5
    nsv5861530copy number variation2nstd209human GRCh38 chr9: 68,352,874-68,356,635 , GRCh37.p13 chr9: 70,967,790-70,971,551 , GRCh37.p13 chr9|NW_003871067.1: 132,322-136,083 PGM5-AS1, PGM5
    nsv5850109copy number variation1nstd209human GRCh38 chr9: 68,467,578-68,468,876 , GRCh37.p13 chr9|NW_003871067.1: 247,026-248,324 , GRCh37.p13 chr9: 71,082,494-71,083,792 PGM5
    nsv5848815copy number variation1nstd209human GRCh37.p13 chr9|NW_003871067.1: 129,958-136,846 , GRCh38 chr9: 68,350,510-68,357,398 , GRCh37.p13 chr9: 70,965,426-70,972,314 PGM5-AS1, LOC102723624, 1 more genes
    nsv5724656mobile element insertion1nstd211human GRCh38 chr9: 68,429,206-68,429,206 , GRCh37.p13 chr9|NW_003871067.1: 208,654-208,654 , GRCh37.p13 chr9: 71,044,122-71,044,122 PGM5
    nsv5637416insertion1nstd207human GRCh38 chr9: 68,502,328-68,502,328 , GRCh37.p13 chr9|NW_003871067.1: 281,776-281,776 , GRCh37.p13 chr9: 71,117,244-71,117,244 PGM5
    nsv5634367insertion1nstd207human GRCh38 chr9: 68,356,407-68,356,407 , GRCh37.p13 chr9: 70,971,323-70,971,323 , GRCh37.p13 chr9|NW_003871067.1: 135,855-135,855 PGM5-AS1, PGM5
    nsv5634221insertion1nstd207human GRCh38 chr9: 68,376,913-68,376,913 , GRCh37.p13 chr9: 70,991,829-70,991,829 , GRCh37.p13 chr9|NW_003871067.1: 156,361-156,361 PGM5, LOC105376070
    nsv5624936insertion1nstd207human GRCh38 chr9: 68,384,241-68,384,241 , GRCh37.p13 chr9|NW_003871067.1: 163,689-163,689 , GRCh37.p13 chr9: 70,999,157-70,999,157 PGM5, LOC105376070
    nsv5604056copy number variation1nstd207human GRCh37.p13 chr9|NW_003871067.1: 196,216-196,489 , GRCh38 chr9: 68,416,768-68,417,041 , GRCh37.p13 chr9: 71,031,684-71,031,957 PGM5
    nsv5597546copy number variation1nstd207human GRCh38 chr9: 68,406,660-68,406,709 , GRCh37.p13 chr9|NW_003871067.1: 186,108-186,157 PGM5
    nsv5597384copy number variation1nstd207human GRCh38 chr9: 68,380,844-68,381,337 , GRCh37.p13 chr9: 70,995,760-70,996,253 , GRCh37.p13 chr9|NW_003871067.1: 160,292-160,785 PGM5, LOC105376070
    nsv5595525copy number variation1nstd207human GRCh38 chr9: 68,369,259-68,369,624 , GRCh37.p13 chr9: 70,984,175-70,984,540 , GRCh37.p13 chr9|NW_003871067.1: 148,707-149,072 PGM5
    nsv5587614copy number variation1nstd207human GRCh38 chr9: 68,358,951-68,359,094 , GRCh37.p13 chr9|NW_003871067.1: 138,399-138,542 , GRCh37.p13 chr9: 70,973,867-70,974,010 PGM5
    nsv5584822copy number variation1nstd207human GRCh38 chr9: 68,416,767-68,417,472 , GRCh37.p13 chr9|NW_003871067.1: 196,215-196,920 , GRCh37.p13 chr9: 71,031,683-71,032,388 PGM5
    nsv5556487mobile element insertion1nstd206human GRCh38 chr9: 68,384,240-68,384,246 , GRCh37.p13 chr9|NW_003871067.1: 163,688-163,694 , GRCh37.p13 chr9: 70,999,156-70,999,162 PGM5, LOC105376070
    nsv5476949copy number variation1nstd206human GRCh37.p13 chr9|NW_003871067.1: 215,000-295,379 , GRCh38 chr9: 68,435,552-68,584,552 , GRCh37.p13 chr9: 71,050,468-71,130,847 LINC01506, TMEM252-DT, 2 more genes
    nsv5475855copy number variation1nstd206human GRCh38 chr9: 68,502,328-68,502,434 , GRCh37.p13 chr9|NW_003871067.1: 281,776-281,882 , GRCh37.p13 chr9: 71,117,244-71,117,350 PGM5
    nsv5474350copy number variation1nstd206human GRCh38 chr9: 68,503,047-68,503,141 , GRCh37.p13 chr9: 71,117,963-71,118,057 , GRCh37.p13 chr9|NW_003871067.1: 282,495-282,589 PGM5
    nsv5247690copy number variation1nstd204human GRCh38.p13 chr9: 68,362,300-68,375,822 , GRCh37.p13 chr9: 70,977,216-70,990,738 , GRCh37.p13 chr9|NW_003871067.1: 141,748-155,270 LOC105376070, PGM5
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