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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929070copy number variation1nstd209human GRCh38 chr19: 10,101,606-10,103,890 , GRCh37.p13 chr19: 10,212,282-10,214,566 ANGPTL6
    nsv5883487copy number variation1nstd209human GRCh38 chr19: 10,102,138-10,103,376 , GRCh37.p13 chr19: 10,212,814-10,214,052 ANGPTL6
    nsv5586008copy number variation1nstd207human GRCh38 chr19: 10,101,606-10,103,890 , GRCh37.p13 chr19: 10,212,282-10,214,566 ANGPTL6
    nsv5533463copy number variation1nstd206human GRCh38 chr19: 10,102,065-10,104,107 , GRCh37.p13 chr19: 10,212,741-10,214,783 ANGPTL6
    nsv5523800copy number variation1nstd206human GRCh38 chr19: 10,101,941-10,103,465 , GRCh37.p13 chr19: 10,212,617-10,214,141 ANGPTL6
    nsv5393089copy number variation1nstd186human GRCh37 chr19: 10,212,340-10,214,565 , GRCh38.p12 chr19: 10,101,664-10,103,889 ANGPTL6
    nsv5391984copy number variation1nstd186human GRCh37 chr19: 10,212,705-10,214,173 , GRCh38.p12 chr19: 10,102,029-10,103,497 ANGPTL6
    nsv5390977copy number variation1nstd186human GRCh37 chr19: 10,212,341-10,214,565 , GRCh38.p12 chr19: 10,101,665-10,103,889 ANGPTL6
    nsv5390672copy number variation1nstd186human GRCh37 chr19: 10,212,797-10,214,714 , GRCh38.p12 chr19: 10,102,121-10,104,038 ANGPTL6
    nsv5326792copy number variation1nstd204human GRCh38.p13 chr19: 10,101,657-10,103,891 , GRCh37.p13 chr19: 10,212,333-10,214,567 ANGPTL6
    nsv5286442copy number variation1nstd204human GRCh38.p13 chr19: 10,101,588-10,103,817 , GRCh37.p13 chr19: 10,212,264-10,214,493 ANGPTL6
    nsv5285518copy number variation1nstd204human GRCh38.p13 chr19: 10,101,601-10,103,900 , GRCh37.p13 chr19: 10,212,277-10,214,576 ANGPTL6
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5282992copy number variation1nstd204human GRCh38.p13 chr19: 10,101,101-10,105,700 , GRCh37.p13 chr19: 10,211,777-10,216,376 PPAN, ANGPTL6, 2 more genes
    nsv5177254mobile element insertion1nstd203human GRCh38 chr19: 10,101,920-10,101,941 , GRCh37.p13 chr19: 10,212,596-10,212,617 ANGPTL6
    nsv5172702mobile element insertion1nstd203human GRCh38 chr19: 10,101,368-10,101,368 , GRCh37.p13 chr19: 10,212,044-10,212,044 ANGPTL6
    nsv5169497mobile element insertion1nstd203human GRCh38 chr19: 10,101,941-10,101,955 , GRCh37.p13 chr19: 10,212,617-10,212,631 ANGPTL6
    nsv5014498copy number variation1nstd200human GRCh38 chr19: 10,102,367-10,133,810 , GRCh37.p13 chr19: 10,213,043-10,244,486 SNORD105B, P2RY11, 6 more genes
    nsv5011584copy number variation1nstd200human GRCh38 chr19: 10,102,025-10,103,497 , GRCh37.p13 chr19: 10,212,701-10,214,173 ANGPTL6
    nsv5011583copy number variation1nstd200human GRCh38 chr19: 10,101,664-10,103,889 , GRCh37.p13 chr19: 10,212,340-10,214,565 ANGPTL6
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