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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128415copy number variation1nstd186human GRCh37 chr18: 77,499,830-77,500,191 , GRCh38.p12 chr18: 79,739,830-79,740,191 CTDP1
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 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
    nsv5946208copy number variation1nstd209human GRCh38 chr18: 79,733,516-79,733,641 , GRCh37.p13 chr18: 77,493,516-77,493,641 CTDP1
    nsv5945721copy number variation1nstd209human GRCh38 chr18: 79,740,970-79,741,249 , GRCh37.p13 chr18: 77,500,970-77,501,249 CTDP1
    nsv5944629copy number variation1nstd209human GRCh38 chr18: 79,694,244-79,694,527 , GRCh37.p13 chr18: 77,454,244-77,454,527 CTDP1
    nsv5943184copy number variation1nstd209human GRCh38 chr18: 79,704,418-79,704,499 , GRCh37.p13 chr18: 77,464,418-77,464,499 CTDP1
    nsv5936067copy number variation1nstd209human GRCh38 chr18: 79,641,572-80,107,313 , GRCh37.p13 chr18: 77,401,572-77,865,197 , KCNG2, 9 more genes
    nsv5933254copy number variation1nstd209human GRCh38 chr18: 79,739,830-79,740,189 , GRCh37.p13 chr18: 77,499,830-77,500,189 CTDP1
    nsv5930026copy number variation1nstd209human GRCh38 chr18: 79,734,524-79,734,610 , GRCh37.p13 chr18: 77,494,524-77,494,610 CTDP1
    nsv5928916copy number variation1nstd209human GRCh38 chr18: 79,692,617-79,692,667 , GRCh37.p13 chr18: 77,452,617-77,452,667 CTDP1
    nsv5885155copy number variation2nstd209human GRCh38 chr18: 79,706,144-79,707,243 , GRCh37.p13 chr18: 77,466,144-77,467,243 CTDP1
    nsv5876623copy number variation2nstd209human GRCh38 chr18: 79,752,325-79,753,800 , GRCh37.p13 chr18: 77,512,325-77,513,800 CTDP1
    nsv5874619copy number variation1nstd209human GRCh38 chr18: 79,651,053-79,682,120 , GRCh37.p13 chr18: 77,411,053-77,442,120 , CTDP1, 1 more genes
    nsv5874292copy number variation1nstd209human GRCh38 chr18: 79,692,206-79,698,769 , GRCh37.p13 chr18: 77,452,206-77,458,769 CTDP1
    nsv5871400copy number variation2nstd209human GRCh38 chr18: 79,704,994-79,707,118 , GRCh37.p13 chr18: 77,464,994-77,467,118 CTDP1
    nsv5869265copy number variation1nstd209human GRCh38 chr18: 79,728,496-79,741,217 , GRCh37.p13 chr18: 77,488,496-77,501,217 CTDP1
    nsv5663901insertion1nstd207human GRCh38 chr18: 79,691,543-79,691,543 , GRCh37.p13 chr18: 77,451,543-77,451,543 CTDP1
    nsv5663606insertion1nstd207human GRCh38 chr18: 79,685,054-79,685,054 , GRCh37.p13 chr18: 77,445,054-77,445,054 , CTDP1
    nsv5662681insertion1nstd207human GRCh38 chr18: 79,687,573-79,687,573 , GRCh37.p13 chr18: 77,447,573-77,447,573 , CTDP1
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