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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4846419copy number variation1nstd200human GRCh37 chr10: 96,560,404-96,564,403 , GRCh38.p12 chr10: 94,800,647-94,804,646 CYP2C19
    nsv4845466copy number variation1nstd200human GRCh37 chr10: 96,403,450-96,521,581 , GRCh38.p12 chr10: 94,643,693-94,761,824 CTBP2P2, CYP2C18, 2 more genes
    nsv4844754copy number variation1nstd200human GRCh37 chr10: 96,524,121-96,524,192 , GRCh38.p12 chr10: 94,764,364-94,764,435 CYP2C19, MTND4P19
    nsv4842042copy number variation1nstd200human GRCh37 chr10: 96,522,199-96,611,261 , GRCh38.p12 chr10: 94,762,442-94,851,504 CYP2C19, MTND4P19
    nsv4841457copy number variation1nstd200human GRCh37 chr10: 96,607,016-96,609,396 , GRCh38.p12 chr10: 94,847,259-94,849,639 CYP2C19
    nsv4838542copy number variation1nstd200human GRCh37 chr10: 96,497,330-96,559,109 , GRCh38.p12 chr10: 94,737,573-94,799,352 MTND4P19, CYP2C19
    nsv4838420copy number variation1nstd200human GRCh37 chr10: 96,613,376-96,613,815 , GRCh38.p12 chr10: 94,853,619-94,854,058 CYP2C19
    nsv4838015copy number variation1nstd200human GRCh37 chr10: 96,533,900-96,542,735 , GRCh38.p12 chr10: 94,774,143-94,782,978 MTND4P19, CYP2C19
    nsv4751589insertion1nstd199human GRCh37 chr10: 96,584,686-96,584,686 , GRCh38.p12 chr10: 94,824,929-94,824,929 CYP2C19
    nsv4729709copy number variation1nstd102humanUncertain significance GRCh37 chr10: 96,140,621-97,222,801 , GRCh38.p12 chr10: 94,380,864-95,463,044 LOC107984257, RPL7AP52, 18 more genes
    nsv4716719mobile element insertion1nstd186human GRCh37 chr10: 96,611,019-96,611,019 , GRCh38.p12 chr10: 94,851,262-94,851,262 CYP2C19
    nsv4618506copy number variation1nstd183human GRCh37 chr10: 96,497,183-96,558,979 , GRCh38.p12 chr10: 94,737,426-94,799,222 CYP2C19, MTND4P19
    nsv4613352copy number variation1nstd183human GRCh37 chr10: 96,497,896-96,567,386 , GRCh38.p12 chr10: 94,738,139-94,807,629 MTND4P19, CYP2C19
    nsv4608480copy number variation1nstd183human GRCh37 chr10: 96,581,094-96,739,268 , GRCh38.p12 chr10: 94,821,337-94,979,511 CYP2C19, CYP2C9, 4 more genes
    nsv4604488copy number variation2nstd183human GRCh37 chr10: 96,534,506-96,649,521 , GRCh38.p12 chr10: 94,774,749-94,889,764 RPL7AP52, MTND4P19, 2 more genes
    nsv4602806copy number variation1nstd183human GRCh37 chr10: 96,403,446-96,521,581 , GRCh38.p12 chr10: 94,643,689-94,761,824 CYP2C18, MTND4P19, 2 more genes
    nsv4598905copy number variation1nstd183human GRCh37 chr10: 96,428,970-96,691,556 , GRCh38.p12 chr10: 94,669,213-94,931,799 CYP2C19, CYP2C18, 4 more genes
    nsv4546620insertion1nstd166human GRCh37.p13 chr10: 96,613,749-96,613,749 , GRCh38.p12 chr10: 94,853,992-94,853,992 CYP2C19
    nsv4528942copy number variation1nstd166human GRCh37.p13 chr10: 96,556,749-96,608,000 , GRCh38.p12 chr10: 94,796,992-94,848,243 CYP2C19
    nsv4528268copy number variation1nstd166human GRCh37.p13 chr10: 96,572,399-96,728,000 , GRCh38.p12 chr10: 94,812,642-94,968,243 CYP2C19, CYP2C9, 4 more genes
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