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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956003insertion1nstd209human GRCh38 chr6: 110,129,596-110,129,596 , GRCh37.p13 chr6: 110,450,799-110,450,799 WASF1
    nsv5891763copy number variation1nstd209human GRCh38 chr6: 110,155,523-110,158,563 , GRCh37.p13 chr6: 110,476,726-110,479,766 WASF1
    nsv5724169mobile element insertion1nstd211human GRCh38 chr6: 110,126,693-110,126,693 , GRCh37.p13 chr6: 110,447,896-110,447,896 WASF1
    nsv5720878mobile element insertion1nstd211human GRCh38 chr6: 110,114,778-110,114,778 , GRCh37.p13 chr6: 110,435,981-110,435,981 WASF1
    nsv5686988mobile element insertion2nstd211human GRCh38 chr6: 110,133,356-110,133,356 , GRCh37.p13 chr6: 110,454,559-110,454,559 WASF1
    nsv5684024mobile element insertion2nstd211human GRCh38 chr6: 110,102,749-110,102,749 , GRCh37.p13 chr6: 110,423,952-110,423,952 WASF1
    nsv5679428mobile element insertion2nstd211human GRCh38 chr6: 110,129,607-110,129,607 , GRCh37.p13 chr6: 110,450,810-110,450,810 WASF1
    nsv5678529mobile element insertion2nstd211human GRCh38 chr6: 110,115,400-110,115,400 , GRCh37.p13 chr6: 110,436,603-110,436,603 WASF1
    nsv5676357mobile element insertion2nstd211human GRCh38 chr6: 110,146,371-110,146,371 , GRCh37.p13 chr6: 110,467,574-110,467,574 WASF1
    nsv5635688insertion1nstd207human GRCh38 chr6: 110,102,734-110,102,734 , GRCh37.p13 chr6: 110,423,937-110,423,937 WASF1
    nsv5629326insertion1nstd207human GRCh38 chr6: 110,129,592-110,129,592 , GRCh37.p13 chr6: 110,450,795-110,450,795 WASF1
    nsv5569001copy number variation1nstd207human GRCh38 chr6: 110,155,523-110,158,563 , GRCh37.p13 chr6: 110,476,726-110,479,766 WASF1
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5549273insertion1nstd206human GRCh38 chr6: 110,129,607-110,129,647 , GRCh37.p13 chr6: 110,450,810-110,450,850 WASF1
    nsv5540511insertion1nstd206human GRCh38 chr6: 110,102,749-110,102,776 , GRCh37.p13 chr6: 110,423,952-110,423,979 WASF1
    nsv5466193copy number variation1nstd206human GRCh38 chr6: 110,132,941-110,136,065 , GRCh37.p13 chr6: 110,454,144-110,457,268 WASF1
    nsv5462021copy number variation1nstd206human GRCh38 chr6: 110,144,790-110,155,000 , GRCh37.p13 chr6: 110,465,993-110,476,203 WASF1
    nsv5460428copy number variation1nstd206human GRCh38 chr6: 110,155,538-110,158,564 , GRCh37.p13 chr6: 110,476,741-110,479,767 WASF1
    nsv5408701mobile element insertion1nstd206human GRCh38 chr6: 110,146,371-110,146,422 , GRCh37.p13 chr6: 110,467,574-110,467,625 WASF1
    nsv5405051mobile element insertion1nstd206human GRCh38 chr6: 110,115,400-110,115,451 , GRCh37.p13 chr6: 110,436,603-110,436,654 WASF1
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