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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7014192copy number variation1nstd229human GRCh38 chr18: 35,372,201-35,378,500 , GRCh37.p13 chr18: 32,952,165-32,958,464 ZNF396
    nsv7010421copy number variation1nstd229human GRCh38 chr18: 35,363,857-35,375,276 , GRCh37.p13 chr18: 32,943,821-32,955,240 ZNF396
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7004753copy number variation1nstd229human GRCh38 chr18: 35,367,949-35,370,395 , GRCh37.p13 chr18: 32,947,913-32,950,359 ZNF396
    nsv7003203copy number variation1nstd229human GRCh38 chr18: 35,371,101-35,378,000 , GRCh37.p13 chr18: 32,951,065-32,957,964 ZNF396
    nsv7002304copy number variation1nstd229human GRCh38 chr18: 35,372,101-35,378,100 , GRCh37.p13 chr18: 32,952,065-32,958,064 ZNF396
    nsv7001466copy number variation1nstd229human GRCh38 chr18: 35,369,022-35,379,697 , GRCh37.p13 chr18: 32,948,986-32,959,661 ZNF396
    nsv7001179copy number variation1nstd229human GRCh38 chr18: 35,360,382-35,366,831 , GRCh37.p13 chr18: 32,940,346-32,946,795 ZNF396
    nsv6535144copy number variation1nstd223human GRCh38 chr18: 35,369,022-35,379,694 , GRCh37.p13 chr18: 32,948,986-32,959,658 ZNF396
    nsv6531505copy number variation1nstd223human GRCh38 chr18: 35,360,382-35,366,828 , GRCh37.p13 chr18: 32,940,346-32,946,792 ZNF396
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133334copy number variation1nstd213human GRCh37 chr18: 32,810,000-34,010,001 , GRCh38.p12 chr18: 35,230,036-36,430,038 GALNT1, ZNF24, 23 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6107779inversion1nstd212human GRCh38 chr18: 34,743,532-36,146,243 , GRCh37.p13 chr18: 32,323,496-33,726,206 , DTNA, 22 more genes
    nsv5937346copy number variation1nstd209human GRCh38 chr18: 35,370,257-35,370,706 , GRCh37.p13 chr18: 32,950,221-32,950,670 ZNF396
    nsv5532582copy number variation1nstd206human GRCh38 chr18: 35,370,237-35,370,727 , GRCh37.p13 chr18: 32,950,201-32,950,691 ZNF396
    nsv5520150copy number variation1nstd206human GRCh38 chr18: 35,372,136-35,378,135 , GRCh37.p13 chr18: 32,952,100-32,958,099 ZNF396
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