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Items: 1 to 20 of 643

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964298insertion1nstd209human GRCh38 chr9: 14,814,031-14,814,031 , GRCh37.p13 chr9: 14,814,029-14,814,029 FREM1
    nsv5962840insertion1nstd209human GRCh38 chr9: 14,877,435-14,877,435 , GRCh37.p13 chr9: 14,877,433-14,877,433 FREM1
    nsv5955027insertion1nstd209human GRCh38 chr9: 14,860,546-14,860,546 , GRCh37.p13 chr9: 14,860,544-14,860,544 FREM1
    nsv5919277copy number variation1nstd209human GRCh38 chr9: 14,860,789-14,860,872 , GRCh37.p13 chr9: 14,860,787-14,860,870 FREM1
    nsv5916392copy number variation1nstd209human GRCh38 chr9: 14,850,336-14,850,434 , GRCh37.p13 chr9: 14,850,334-14,850,432 FREM1, RNU6-1260P
    nsv5710253mobile element insertion1nstd211human GRCh38 chr9: 14,789,288-14,789,288 , GRCh37.p13 chr9: 14,789,286-14,789,286 FREM1
    nsv5709105mobile element insertion1nstd211human GRCh38 chr9: 14,811,132-14,811,132 , GRCh37.p13 chr9: 14,811,130-14,811,130 FREM1
    nsv5707933mobile element insertion2nstd211human GRCh38 chr9: 14,904,546-14,904,546 , GRCh37.p13 chr9: 14,904,544-14,904,544 FREM1
    nsv5706089mobile element insertion2nstd211human GRCh38 chr9: 14,877,447-14,877,447 , GRCh37.p13 chr9: 14,877,445-14,877,445 FREM1
    nsv5701928mobile element insertion2nstd211human GRCh38 chr9: 14,901,595-14,901,595 , GRCh37.p13 chr9: 14,901,593-14,901,593 FREM1
    nsv5640169insertion1nstd207human GRCh38 chr9: 14,877,435-14,877,435 , GRCh37.p13 chr9: 14,877,433-14,877,433 FREM1
    nsv5637714insertion1nstd207human GRCh38 chr9: 14,901,581-14,901,581 , GRCh37.p13 chr9: 14,901,579-14,901,579 FREM1
    nsv5637371insertion1nstd207human GRCh38 chr9: 14,778,681-14,778,681 , GRCh37.p13 chr9: 14,778,679-14,778,679 FREM1
    nsv5633896insertion1nstd207human GRCh38 chr9: 14,860,856-14,860,856 , GRCh37.p13 chr9: 14,860,854-14,860,854 FREM1
    nsv5631823insertion1nstd207human GRCh38 chr9: 14,860,546-14,860,546 , GRCh37.p13 chr9: 14,860,544-14,860,544 FREM1
    nsv5630027insertion1nstd207human GRCh38 chr9: 14,825,561-14,825,561 , GRCh37.p13 chr9: 14,825,559-14,825,559 FREM1
    nsv5627414insertion1nstd207human GRCh38 chr9: 14,860,928-14,860,928 , GRCh37.p13 chr9: 14,860,926-14,860,926 FREM1
    nsv5604514copy number variation1nstd207human GRCh38 chr9: 14,861,038-14,861,117 , GRCh37.p13 chr9: 14,861,036-14,861,115 FREM1
    nsv5602509copy number variation1nstd207human GRCh38 chr9: 14,861,046-14,861,217 , GRCh37.p13 chr9: 14,861,044-14,861,215 FREM1
    nsv5593835copy number variation1nstd207human GRCh38 chr9: 14,850,336-14,850,434 , GRCh37.p13 chr9: 14,850,334-14,850,432 FREM1, RNU6-1260P
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