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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310355copy number variation1nstd102humanPathogenic GRCh37 chr18: 29,115,223-29,118,951 , GRCh38.p12 chr18: 31,535,260-31,538,988 DSG2
    nsv7093574delins1nstd102humanPathogenic GRCh37 chr18: 29,104,749-29,104,778 , GRCh38 chr18: 31,524,786-31,524,815 DSG2
    nsv6310255copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 29,099,325-29,099,910 , GRCh38.p12 chr18: 31,519,362-31,519,947 DSG2
    nsv6310208copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 29,099,746-29,099,920 , GRCh38.p12 chr18: 31,519,783-31,519,957 DSG2
    nsv4681895copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 29,099,756-29,099,910 , GRCh38.p12 chr18: 31,519,793-31,519,947 DSG2
    nsv6998279copy number variation1nstd229human GRCh38 chr18: 31,500,649-31,509,053 , GRCh37.p13 chr18: 29,080,612-29,089,016 DSG2
    nsv7001124copy number variation1nstd229human GRCh38 chr18: 31,490,540-31,496,424 , GRCh37.p13 chr18: 29,070,503-29,076,387 DSG2
    nsv7013331copy number variation1nstd229human GRCh38 chr18: 31,554,787-31,558,082 , GRCh37.p13 chr18: 29,134,750-29,138,045 DSG2-AS1
    nsv5524104copy number variation1nstd206human GRCh38 chr18: 31,528,628-31,528,847 , GRCh37.p13 chr18: 29,108,591-29,108,810 DSG2
    nsv5526156copy number variation1nstd206human GRCh38 chr18: 31,526,326-31,526,431 , GRCh37.p13 chr18: 29,106,289-29,106,394 DSG2
    nsv5519081copy number variation1nstd206human GRCh38 chr18: 31,538,984-31,539,044 , GRCh37.p13 chr18: 29,118,947-29,119,007 DSG2
    nsv6029363copy number variation1nstd212human GRCh38 chr18: 31,525,321-31,525,947 , GRCh37.p13 chr18: 29,105,284-29,105,910 DSG2
    nsv4859144copy number variation1nstd200human GRCh37 chr18: 29,085,899-29,086,941 , GRCh38.p12 chr18: 31,505,936-31,506,978 DSG2
    nsv5011178copy number variation1nstd200human GRCh38 chr18: 31,505,929-31,506,985 , GRCh37.p13 chr18: 29,085,892-29,086,948 DSG2
    nsv5011179copy number variation1nstd200human GRCh38 chr18: 31,517,695-31,518,700 , GRCh37.p13 chr18: 29,097,658-29,098,663 DSG2
    nsv4859145copy number variation1nstd200human GRCh37 chr18: 29,097,658-29,098,663 , GRCh38.p12 chr18: 31,517,695-31,518,700 DSG2
    nsv5011180copy number variation1nstd200human GRCh38 chr18: 31,531,926-31,532,040 , GRCh37.p13 chr18: 29,111,889-29,112,003 DSG2
    nsv5942329copy number variation1nstd209human GRCh38 chr18: 31,526,323-31,526,430 , GRCh37.p13 chr18: 29,106,286-29,106,393 DSG2
    nsv4261385copy number variation1nstd166human GRCh37.p13 chr18: 29,080,612-29,089,009 , GRCh38.p12 chr18: 31,500,649-31,509,046 DSG2
    nsv4259802copy number variation1nstd166human GRCh37.p13 chr18: 29,085,907-29,086,939 , GRCh38.p12 chr18: 31,505,944-31,506,976 DSG2
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