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Items: 1 to 20 of 547

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950149insertion1nstd209human GRCh38 chr9: 15,167,005-15,167,005 , GRCh37.p13 chr9: 15,167,003-15,167,003 , TTC39B
    nsv5918411copy number variation1nstd209human GRCh38 chr9: 15,285,165-15,285,750 , GRCh37.p13 chr9: 15,285,163-15,285,748 TTC39B
    nsv5917725copy number variation1nstd209human GRCh38 chr9: 15,189,397-15,189,525 , GRCh37.p13 chr9: 15,189,395-15,189,523 TTC39B
    nsv5916862copy number variation1nstd209human GRCh38 chr9: 15,205,674-15,206,302 , GRCh37.p13 chr9: 15,205,672-15,206,300 TTC39B
    nsv5710925mobile element insertion2nstd211human GRCh38 chr9: 15,168,431-15,168,431 , GRCh37.p13 chr9: 15,168,429-15,168,429 TTC39B
    nsv5710345mobile element insertion2nstd211human GRCh38 chr9: 15,283,537-15,283,537 , GRCh37.p13 chr9: 15,283,535-15,283,535 TTC39B
    nsv5702078mobile element insertion2nstd211human GRCh38 chr9: 15,223,587-15,223,587 , GRCh37.p13 chr9: 15,223,585-15,223,585 TTC39B
    nsv5698442mobile element insertion1nstd211human GRCh38 chr9: 15,173,093-15,173,093 , GRCh37.p13 chr9: 15,173,091-15,173,091 TTC39B
    nsv5696144mobile element insertion2nstd211human GRCh38 chr9: 15,187,096-15,187,096 , GRCh37.p13 chr9: 15,187,094-15,187,094 TTC39B
    nsv5694637mobile element insertion1nstd211human GRCh38 chr9: 15,218,632-15,218,632 , GRCh37.p13 chr9: 15,218,630-15,218,630 TTC39B
    nsv5626635insertion1nstd207human GRCh38 chr9: 15,234,395-15,234,395 , GRCh37.p13 chr9: 15,234,393-15,234,393 TTC39B
    nsv5490455copy number variation1nstd206human GRCh38 chr9: 15,164,287-15,164,828 , GRCh37.p13 chr9: 15,164,285-15,164,826 TTC39B
    nsv5490298copy number variation1nstd206human GRCh38 chr9: 15,233,766-15,234,152 , GRCh37.p13 chr9: 15,233,764-15,234,150 TTC39B
    nsv5487587copy number variation1nstd206human GRCh38 chr9: 15,218,888-15,221,581 , GRCh37.p13 chr9: 15,218,886-15,221,579 TTC39B
    nsv5486017copy number variation1nstd206human GRCh38 chr9: 15,163,321-15,205,245 , GRCh37.p13 chr9: 15,163,319-15,205,243 TTC39B
    nsv5482407copy number variation1nstd206human GRCh38 chr9: 15,205,676-15,206,303 , GRCh37.p13 chr9: 15,205,674-15,206,301 TTC39B
    nsv5479813copy number variation1nstd206human GRCh38 chr9: 15,198,300-15,200,800 , GRCh37.p13 chr9: 15,198,298-15,200,798 TTC39B
    nsv5479492copy number variation1nstd206human GRCh38 chr9: 15,285,140-15,285,751 , GRCh37.p13 chr9: 15,285,138-15,285,749 TTC39B
    nsv5479047copy number variation1nstd206human GRCh38 chr9: 15,189,398-15,189,544 , GRCh37.p13 chr9: 15,189,396-15,189,542 TTC39B
    nsv5478651copy number variation1nstd206human GRCh38 chr9: 15,285,165-15,285,751 , GRCh37.p13 chr9: 15,285,163-15,285,749 TTC39B
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