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Items: 1 to 20 of 840

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956259insertion1nstd209human GRCh38 chr4: 56,200,022-56,200,022 , GRCh37.p13 chr4: 57,066,188-57,066,188 CRACD
    nsv5897072copy number variation1nstd209human GRCh38 chr4: 56,214,399-56,214,816 , GRCh37.p13 chr4: 57,080,565-57,080,982 CRACD
    nsv5896187copy number variation1nstd209human GRCh38 chr4: 56,197,778-56,206,034 , GRCh37.p13 chr4: 57,063,944-57,072,200 CRACD
    nsv5889756copy number variation1nstd209human GRCh38 chr4: 56,079,272-56,079,332 , GRCh37.p13 chr4: 56,945,438-56,945,498 CRACD
    nsv5839689copy number variation1nstd209human GRCh38 chr4: 56,197,075-56,199,374 , GRCh37.p13 chr4: 57,063,241-57,065,540 CRACD
    nsv5839075copy number variation1nstd209human GRCh38 chr4: 56,196,875-56,205,074 , GRCh37.p13 chr4: 57,063,041-57,071,240 CRACD
    nsv5726930mobile element insertion1nstd211human GRCh38 chr4: 56,190,580-56,190,580 , GRCh37.p13 chr4: 57,056,746-57,056,746 CRACD
    nsv5721577mobile element insertion1nstd211human GRCh38 chr4: 56,320,402-56,320,402 , GRCh37.p13 chr4: 57,186,568-57,186,568 CRACD, MRPL22P1
    nsv5716232mobile element insertion1nstd211human GRCh38 chr4: 56,188,877-56,188,877 , GRCh37.p13 chr4: 57,055,043-57,055,043 CRACD
    nsv5715726mobile element insertion1nstd211human GRCh38 chr4: 56,135,646-56,135,646 , GRCh37.p13 chr4: 57,001,812-57,001,812 CRACD
    nsv5715021mobile element insertion1nstd211human GRCh38 chr4: 56,251,896-56,251,896 , GRCh37.p13 chr4: 57,118,062-57,118,062 CRACD
    nsv5687276mobile element insertion2nstd211human GRCh38 chr4: 56,200,041-56,200,041 , GRCh37.p13 chr4: 57,066,207-57,066,207 CRACD
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5623870insertion1nstd207human GRCh38 chr4: 56,214,681-56,214,681 , GRCh37.p13 chr4: 57,080,847-57,080,847 CRACD
    nsv5618897insertion1nstd207human GRCh38 chr4: 56,183,287-56,183,287 , GRCh37.p13 chr4: 57,049,453-57,049,453 CRACD
    nsv5616636insertion1nstd207human GRCh38 chr4: 56,183,288-56,183,288 , GRCh37.p13 chr4: 57,049,454-57,049,454 CRACD
    nsv5570443copy number variation1nstd207human GRCh38 chr4: 56,112,782-56,112,839 , GRCh37.p13 chr4: 56,978,948-56,979,005 CRACD
    nsv5565858copy number variation1nstd207human GRCh38 chr4: 56,057,799-56,057,995 , GRCh37.p13 chr4: 56,923,965-56,924,161 CRACD
    nsv5560588mobile element insertion1nstd206human GRCh38 chr4: 56,251,896-56,251,947 , GRCh37.p13 chr4: 57,118,062-57,118,113 CRACD
    nsv5557875sequence alteration1nstd206human GRCh38 chr4: 56,179,761-56,589,194 , GRCh37.p13 chr4: 57,045,927-57,455,360 , PPAT, 12 more genes
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