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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951746insertion1nstd209human GRCh38 chr10: 96,557,461-96,557,461 , GRCh37.p13 chr10: 98,317,218-98,317,218 TM9SF3
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5909484copy number variation1nstd209human GRCh38 chr10: 96,525,750-96,525,801 , GRCh37.p13 chr10: 98,285,507-98,285,558 TM9SF3
    nsv5723251mobile element insertion1nstd211human GRCh38 chr10: 96,566,765-96,566,765 , GRCh37.p13 chr10: 98,326,522-98,326,522 TM9SF3
    nsv5628536insertion1nstd207human GRCh38 chr10: 96,557,461-96,557,461 , GRCh37.p13 chr10: 98,317,218-98,317,218 TM9SF3
    nsv5545054insertion1nstd206human GRCh38 chr10: 96,557,466-96,557,512 , GRCh37.p13 chr10: 98,317,223-98,317,269 TM9SF3
    nsv5486241copy number variation1nstd206human GRCh38 chr10: 96,521,588-96,521,862 , GRCh37.p13 chr10: 98,281,345-98,281,619 TM9SF3
    nsv5348018translocation1nstd200human GRCh38 chr10: 96,521,862-96,521,862 , GRCh38 chr10: 96,521,588-96,521,588 , GRCh37.p13 chr10: 98,281,345-98,281,345 , GRCh37.p13 chr10: 98,281,619-98,281,619 TM9SF3
    nsv5131699mobile element insertion1nstd203human GRCh38 chr10: 96,530,696-96,530,711 , GRCh37.p13 chr10: 98,290,453-98,290,468 TM9SF3
    nsv5128683mobile element insertion1nstd203human GRCh38 chr10: 96,524,904-96,524,921 , GRCh37.p13 chr10: 98,284,661-98,284,678 TM9SF3
    nsv4836401copy number variation1nstd200human GRCh37 chr10: 98,281,345-98,281,619 , GRCh38.p12 chr10: 96,521,588-96,521,862 TM9SF3
    nsv4829564copy number variation1nstd200human GRCh37 chr10: 98,342,765-98,343,666 , GRCh38.p12 chr10: 96,583,008-96,583,909 TM9SF3
    nsv4763956insertion1nstd199human GRCh37 chr10: 98,317,218-98,317,218 , GRCh38.p12 chr10: 96,557,461-96,557,461 TM9SF3
    nsv4617225copy number variation1nstd183human GRCh37 chr10: 98,287,089-98,287,220 , GRCh38.p12 chr10: 96,527,332-96,527,463 TM9SF3
    nsv4611970copy number variation1nstd183human GRCh37 chr10: 98,346,465-98,346,711 , GRCh38.p12 chr10: 96,586,708-96,586,954 TM9SF3, LOC105378443
    nsv4600325copy number variation1nstd183human GRCh37 chr10: 98,279,604-98,280,809 , GRCh38.p12 chr10: 96,519,847-96,521,052 TM9SF3
    nsv4574637mobile element insertion1nstd166human GRCh37.p13 chr10: 98,341,629-98,341,629 , GRCh38.p12 chr10: 96,581,872-96,581,872 TM9SF3
    nsv4497547mobile element insertion1nstd166human GRCh37.p13 chr10: 98,322,012-98,322,012 , GRCh38.p12 chr10: 96,562,255-96,562,255 TM9SF3
    nsv4487396mobile element insertion1nstd166human GRCh37.p13 chr10: 98,290,453-98,290,453 , GRCh38.p12 chr10: 96,530,696-96,530,696 TM9SF3
    nsv4455800copy number variation1nstd102humanUncertain significance GRCh37 chr10: 98,225,031-98,337,963 , GRCh38.p12 chr10: 96,465,274-96,578,206 TLL2, TM9SF3, 1 more genes
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