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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126752copy number variation1nstd186human GRCh37 chr19: 45,473,113-45,474,257 , GRCh38.p12 chr19: 44,969,856-44,971,000 CLPTM1
    nsv5938156copy number variation1nstd209human GRCh38 chr19: 44,968,604-44,968,666 , GRCh37.p13 chr19: 45,471,861-45,471,923 CLPTM1
    nsv5933503copy number variation1nstd209human GRCh38 chr19: 44,969,848-44,970,990 , GRCh37.p13 chr19: 45,473,105-45,474,247 CLPTM1
    nsv5870679copy number variation1nstd209human GRCh38 chr19: 44,969,832-44,971,031 , GRCh37.p13 chr19: 45,473,089-45,474,288 CLPTM1
    nsv5591842copy number variation1nstd207human GRCh38 chr19: 44,969,848-44,970,990 , GRCh37.p13 chr19: 45,473,105-45,474,247 CLPTM1
    nsv5526002copy number variation1nstd206human GRCh38 chr19: 44,965,271-44,998,775 , GRCh37.p13 chr19: 45,468,528-45,502,033 CLPTM1
    nsv5519005copy number variation1nstd206human GRCh38 chr19: 44,969,779-44,971,165 , GRCh37.p13 chr19: 45,473,036-45,474,422 CLPTM1
    nsv5391485copy number variation1nstd186human GRCh37 chr19: 45,473,234-45,473,919 , GRCh38.p12 chr19: 44,969,977-44,970,662 CLPTM1
    nsv5389756copy number variation2nstd186human GRCh37 chr19: 45,473,182-45,474,237 , GRCh38.p12 chr19: 44,969,925-44,970,980 CLPTM1
    nsv5382492mobile element deletion1nstd186human GRCh37 chr19: 45,473,655-45,473,959 , GRCh38.p12 chr19: 44,970,398-44,970,702 CLPTM1
    nsv5359836translocation1nstd200human GRCh38 chr19: 44,968,667-44,968,667 , GRCh38 chr19: 44,968,608-44,968,608 , GRCh37.p13 chr19: 45,471,865-45,471,865 , GRCh37.p13 chr19: 45,471,924-45,471,924 CLPTM1
    nsv5327815copy number variation1nstd204human GRCh38.p13 chr19: 44,969,917-44,970,988 , GRCh37.p13 chr19: 45,473,174-45,474,245 CLPTM1
    nsv5293580copy number variation1nstd204human GRCh38.p13 chr19: 44,969,732-44,971,031 , GRCh37.p13 chr19: 45,472,989-45,474,288 CLPTM1
    nsv5285262copy number variation1nstd204human GRCh38.p13 chr19: 44,969,801-44,971,000 , GRCh37.p13 chr19: 45,473,058-45,474,257 CLPTM1
    nsv5024711copy number variation1nstd200human GRCh38 chr19: 44,969,779-44,971,096 , GRCh37.p13 chr19: 45,473,036-45,474,353 CLPTM1
    nsv5024709copy number variation1nstd200human GRCh38 chr19: 44,901,622-44,953,076 , GRCh37.p13 chr19: 45,404,879-45,456,333 APOC1, APOC2, 6 more genes
    nsv5020664copy number variation1nstd200human GRCh38 chr19: 44,969,975-44,970,662 , GRCh37.p13 chr19: 45,473,232-45,473,919 CLPTM1
    nsv5020663copy number variation1nstd200human GRCh38 chr19: 44,969,925-44,970,980 , GRCh37.p13 chr19: 45,473,182-45,474,237 CLPTM1
    nsv5020662copy number variation1nstd200human GRCh38 chr19: 44,966,177-44,967,377 , GRCh37.p13 chr19: 45,469,434-45,470,634 CLPTM1
    nsv4907548mobile element deletion1nstd200human GRCh38 chr19: 44,970,396-44,970,703 , GRCh37.p13 chr19: 45,473,653-45,473,960 CLPTM1
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