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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128428copy number variation1nstd186human GRCh37 chr18: 52,447,278-52,447,559 , GRCh38.p12 chr18: 54,780,047-54,780,328 RAB27B
    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
    nsv5972286insertion1nstd209human GRCh38 chr18: 54,873,656-54,873,656 , GRCh37.p13 chr18: 52,540,887-52,540,887 RAB27B
    nsv5941895copy number variation1nstd209human GRCh38 chr18: 54,891,266-54,891,424 , GRCh37.p13 chr18: 52,558,497-52,558,655 RAB27B
    nsv5939695copy number variation1nstd209human GRCh38 chr18: 54,872,309-54,874,215 , GRCh37.p13 chr18: 52,539,540-52,541,446 RAB27B
    nsv5937547copy number variation1nstd209human GRCh38 chr18: 54,730,224-54,730,310 , GRCh37.p13 chr18: 52,397,455-52,397,541 RAB27B
    nsv5930289copy number variation1nstd209human GRCh38 chr18: 54,834,719-54,836,924 , GRCh37.p13 chr18: 52,501,950-52,504,155 RAB27B
    nsv5927614copy number variation1nstd209human GRCh38 chr18: 54,723,998-54,726,894 , GRCh37.p13 chr18: 52,391,229-52,394,125 RAB27B
    nsv5881406copy number variation1nstd209human GRCh38 chr18: 54,723,958-54,726,857 , GRCh37.p13 chr18: 52,391,189-52,394,088 RAB27B
    nsv5879139copy number variation1nstd209human GRCh38 chr18: 54,834,714-54,836,913 , GRCh37.p13 chr18: 52,501,945-52,504,144 RAB27B
    nsv5871005copy number variation2nstd209human GRCh38 chr18: 54,889,506-54,890,505 , GRCh37.p13 chr18: 52,556,737-52,557,736 RAB27B
    nsv5704542mobile element insertion2nstd211human GRCh38 chr18: 54,873,656-54,873,656 , GRCh37.p13 chr18: 52,540,887-52,540,887 RAB27B
    nsv5655348insertion1nstd207human GRCh38 chr18: 54,780,326-54,780,326 , GRCh37.p13 chr18: 52,447,557-52,447,557 RAB27B
    nsv5590629copy number variation1nstd207human GRCh38 chr18: 54,779,966-54,780,325 , GRCh37.p13 chr18: 52,447,197-52,447,556 RAB27B
    nsv5586763copy number variation1nstd207human GRCh38 chr18: 54,834,719-54,836,924 , GRCh37.p13 chr18: 52,501,950-52,504,155 RAB27B
    nsv5553703insertion1nstd206human GRCh38 chr18: 54,807,600-54,807,607 , GRCh37.p13 chr18: 52,474,831-52,474,838 RAB27B
    nsv5533220copy number variation1nstd206human GRCh38 chr18: 54,813,160-54,819,533 , GRCh37.p13 chr18: 52,480,391-52,486,764 RAB27B
    nsv5530713copy number variation1nstd206human GRCh38 chr18: 54,834,723-54,836,925 , GRCh37.p13 chr18: 52,501,954-52,504,156 RAB27B
    nsv5529801copy number variation1nstd206human GRCh38 chr18: 54,779,997-54,780,377 , GRCh37.p13 chr18: 52,447,228-52,447,608 RAB27B
    nsv5529722copy number variation1nstd206human GRCh38 chr18: 54,891,269-54,891,425 , GRCh37.p13 chr18: 52,558,500-52,558,656 RAB27B
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