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Items: 1 to 20 of 415

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925637copy number variation1nstd209human GRCh38 chr8: 110,975,842-110,981,579 , GRCh37.p13 chr8: 111,988,071-111,993,808 LINC01608
    nsv5864178copy number variation1nstd209human GRCh38 chr8: 110,976,303-110,981,778 , GRCh37.p13 chr8: 111,988,532-111,994,007 LINC01608
    nsv5858943copy number variation1nstd209human GRCh38 chr8: 110,970,078-110,971,727 , GRCh37.p13 chr8: 111,982,307-111,983,956 LINC01608
    nsv5488922copy number variation1nstd206human GRCh38 chr8: 110,993,768-111,394,168 , GRCh37.p13 chr8: 112,005,997-112,406,397 EEF1A1P37, LINC01608, 6 more genes
    nsv5484388copy number variation1nstd206human GRCh38 chr8: 110,975,842-110,981,580 , GRCh37.p13 chr8: 111,988,071-111,993,809 LINC01608
    nsv5311562copy number variation1nstd204human GRCh38.p13 chr8: 110,975,836-110,981,583 , GRCh37.p13 chr8: 111,988,065-111,993,812 LINC01608
    nsv5258867copy number variation1nstd204human GRCh38.p13 chr8: 110,995,001-110,998,400 , GRCh37.p13 chr8: 112,007,230-112,010,629 LINC01608
    nsv5257619copy number variation1nstd204human GRCh38.p13 chr8: 110,968,378-110,969,877 , GRCh37.p13 chr8: 111,980,607-111,982,106 LINC01608
    nsv5257315copy number variation1nstd204human GRCh38.p13 chr8: 110,975,353-110,981,478 , GRCh37.p13 chr8: 111,987,582-111,993,707 LINC01608
    nsv5253245copy number variation1nstd204human GRCh38.p13 chr8: 110,966,601-110,974,700 , GRCh37.p13 chr8: 111,978,830-111,986,929 LINC01608
    nsv5250537copy number variation1nstd204human GRCh38.p13 chr8: 111,016,601-111,020,300 , GRCh37.p13 chr8: 112,028,830-112,032,529 LINC01608
    nsv5195620mobile element insertion1nstd203human GRCh38 chr8: 110,951,068-110,951,081 , GRCh37.p13 chr8: 111,963,297-111,963,310 LINC01608
    nsv5117548mobile element insertion1nstd203human GRCh38 chr8: 111,019,176-111,019,194 , GRCh37.p13 chr8: 112,031,405-112,031,423 LINC01608
    nsv5108396mobile element insertion1nstd203human GRCh38 chr8: 110,939,659-110,939,674 , GRCh37.p13 chr8: 111,951,888-111,951,903 LINC01608
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965719copy number variation1nstd200human GRCh38 chr8: 110,912,963-111,174,643 , GRCh37.p13 chr8: 111,925,192-112,186,872 LINC01609, MTCO1P47, 3 more genes
    nsv4965716copy number variation1nstd200human GRCh38 chr8: 110,370,859-111,338,035 , GRCh37.p13 chr8: 111,383,088-112,350,264 EEF1A1P37, LOC105375705, 8 more genes
    nsv4961908copy number variation1nstd200human GRCh38 chr8: 111,001,935-111,010,623 , GRCh37.p13 chr8: 112,014,164-112,022,852 LINC01608
    nsv4961907copy number variation1nstd200human GRCh38 chr8: 110,975,842-110,981,580 , GRCh37.p13 chr8: 111,988,071-111,993,809 LINC01608
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