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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127563copy number variation1nstd186human GRCh37 chr18: 28,677,393-28,677,902 , GRCh38.p12 chr18: 31,097,430-31,097,939 DSC2
    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
    nsv5931591copy number variation1nstd209human GRCh38 chr18: 31,097,335-31,097,922 , GRCh37.p13 chr18: 28,677,298-28,677,885 DSC2
    nsv5713436mobile element insertion1nstd211human GRCh38 chr18: 31,078,644-31,078,644 , GRCh37.p13 chr18: 28,658,610-28,658,610 DSC2
    nsv5598666copy number variation1nstd207human GRCh38 chr18: 31,097,305-31,097,931 , GRCh37.p13 chr18: 28,677,268-28,677,894 DSC2
    nsv5521330copy number variation1nstd206human GRCh38 chr18: 31,097,410-31,097,959 , GRCh37.p13 chr18: 28,677,373-28,677,922 DSC2
    nsv5425064mobile element insertion1nstd206human GRCh38 chr18: 31,078,644-31,078,695 , GRCh37.p13 chr18: 28,658,610-28,658,661 DSC2
    nsv5391893copy number variation1nstd186human GRCh37 chr18: 28,677,507-28,677,902 , GRCh38.p12 chr18: 31,097,544-31,097,939 DSC2
    nsv5391345copy number variation1nstd186human GRCh37 chr18: 28,677,268-28,677,901 , GRCh38.p12 chr18: 31,097,305-31,097,938 DSC2
    nsv5322177copy number variation1nstd204human GRCh38.p13 chr18: 31,097,271-31,097,968 , GRCh37.p13 chr18: 28,677,234-28,677,931 DSC2
    nsv5024038copy number variation1nstd200human GRCh38 chr18: 28,435,232-32,096,725 , GRCh37.p13 chr18: 26,015,196-29,676,688 DSC2, LOC100287539, 35 more genes
    nsv5011156copy number variation1nstd200human GRCh38 chr18: 31,097,859-31,098,880 , GRCh37.p13 chr18: 28,677,822-28,678,843 DSC2
    nsv5011155copy number variation1nstd200human GRCh38 chr18: 31,069,123-31,069,225 , GRCh37.p13 chr18: 28,649,089-28,649,191 DSC2
    nsv5011154copy number variation1nstd200human GRCh38 chr18: 31,066,602-31,066,883 , GRCh37.p13 chr18: 28,646,568-28,646,849 DSC2
    nsv4859133copy number variation1nstd200human GRCh37 chr18: 28,677,501-28,677,946 , GRCh38.p12 chr18: 31,097,538-31,097,983 DSC2
    nsv4859132copy number variation1nstd200human GRCh37 chr18: 28,677,267-28,677,902 , GRCh38.p12 chr18: 31,097,304-31,097,939 DSC2
    nsv4729939copy number variation1nstd102humanUncertain significance GRCh37 chr18: 25,329,706-29,734,723 , GRCh38.p12 chr18: 27,749,742-32,154,760 SLC25A52, LOC105372043, 37 more genes
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
    nsv4683807copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 28,647,971-28,650,826 , GRCh38.p12 chr18: 31,068,005-31,070,860 DSC2
    nsv4682967copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,971-28,673,616 , GRCh38.p12 chr18: 31,068,005-31,093,653 DSC2
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