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Items: 1 to 20 of 1921

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964489insertion1nstd209human GRCh38 chr9: 6,780,313-6,780,313 , GRCh37.p13 chr9: 6,780,313-6,780,313 KDM4C
    nsv5961343insertion1nstd209human GRCh38 chr9: 7,019,736-7,019,736 , GRCh37.p13 chr9: 7,019,736-7,019,736 KDM4C
    nsv5954620insertion1nstd209human GRCh38 chr9: 6,926,341-6,926,341 , GRCh37.p13 chr9: 6,926,341-6,926,341 KDM4C
    nsv5948639insertion1nstd209human GRCh38 chr9: 7,035,328-7,035,328 , GRCh37.p13 chr9: 7,035,328-7,035,328 KDM4C
    nsv5926754copy number variation1nstd209human GRCh38 chr9: 6,720,174-6,720,511 , GRCh37.p13 chr9: 6,720,174-6,720,511 KDM4C
    nsv5926620copy number variation1nstd209human GRCh38 chr9: 6,766,693-6,768,245 , GRCh37.p13 chr9: 6,766,693-6,768,245 KDM4C
    nsv5925191copy number variation1nstd209human GRCh38 chr9: 6,913,194-6,913,272 , GRCh37.p13 chr9: 6,913,194-6,913,272 KDM4C
    nsv5923945copy number variation1nstd209human GRCh38 chr9: 7,019,720-7,020,583 , GRCh37.p13 chr9: 7,019,720-7,020,583 KDM4C
    nsv5922263copy number variation1nstd209human GRCh38 chr9: 6,729,119-6,730,105 , GRCh37.p13 chr9: 6,729,119-6,730,105 KDM4C
    nsv5922070copy number variation1nstd209human GRCh38 chr9: 6,672,922-6,746,487 , GRCh37.p13 chr9: 6,672,922-6,746,487 KDM4C, RPL35AP20, 2 more genes
    nsv5920303copy number variation1nstd209human GRCh38 chr9: 6,888,773-6,889,086 , GRCh37.p13 chr9: 6,888,773-6,889,086 KDM4C
    nsv5919400copy number variation1nstd209human GRCh38 chr9: 6,797,955-6,799,505 , GRCh37.p13 chr9: 6,797,955-6,799,505 KDM4C
    nsv5917917copy number variation1nstd209human GRCh38 chr9: 6,978,401-6,978,656 , GRCh37.p13 chr9: 6,978,401-6,978,656 KDM4C
    nsv5917613copy number variation1nstd209human GRCh38 chr9: 6,999,377-6,999,683 , GRCh37.p13 chr9: 6,999,377-6,999,683 KDM4C
    nsv5916356copy number variation1nstd209human GRCh38 chr9: 7,043,306-7,043,365 , GRCh37.p13 chr9: 7,043,306-7,043,365 KDM4C
    nsv5914676copy number variation1nstd209human GRCh38 chr9: 6,880,487-6,882,526 , GRCh37.p13 chr9: 6,880,487-6,882,526 KDM4C
    nsv5913002copy number variation1nstd209human GRCh38 chr9: 6,738,997-6,746,523 , GRCh37.p13 chr9: 6,738,997-6,746,523 KDM4C
    nsv5912932copy number variation1nstd209human GRCh38 chr9: 6,752,035-6,752,355 , GRCh37.p13 chr9: 6,752,035-6,752,355 KDM4C
    nsv5912870copy number variation1nstd209human GRCh38 chr9: 7,019,697-7,019,765 , GRCh37.p13 chr9: 7,019,697-7,019,765 KDM4C
    nsv5911619copy number variation1nstd209human GRCh38 chr9: 7,024,103-7,024,251 , GRCh37.p13 chr9: 7,024,103-7,024,251 KDM4C
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