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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976512inversion1nstd209human GRCh38 chr7: 5,976,108-6,745,714 , GRCh37.p13 chr7: 6,015,739-6,785,345 PMS2, RAC1, 22 more genes
    nsv5926672copy number variation1nstd209human GRCh38 chr7: 6,463,881-6,464,016 , GRCh37.p13 chr7: 6,503,512-6,503,647 KDELR2
    nsv5919129copy number variation1nstd209human GRCh38 chr7: 6,469,203-6,469,524 , GRCh37.p13 chr7: 6,508,834-6,509,155 KDELR2
    nsv5911322copy number variation1nstd209human GRCh38 chr7: 6,421,670-7,105,388 , GRCh37.p13 chr7: 6,461,301-7,145,019 , GRID2IP, 25 more genes
    nsv5909870copy number variation1nstd209human GRCh38 chr7: 6,452,986-6,460,019 , GRCh37.p13 chr7: 6,492,617-6,499,650 KDELR2
    nsv5847299copy number variation1nstd209human GRCh38 chr7: 6,458,797-6,462,096 , GRCh37.p13 chr7: 6,498,428-6,501,727 KDELR2
    nsv5690727mobile element insertion1nstd211human GRCh38 chr7: 6,480,708-6,480,708 , GRCh37.p13 chr7: 6,520,339-6,520,339 KDELR2
    nsv5674676mobile element insertion1nstd211human GRCh38 chr7: 6,476,838-6,476,838 , GRCh37.p13 chr7: 6,516,469-6,516,469 KDELR2
    nsv5667605inversion1nstd207human GRCh37.p13 chr7: 6,028,678-6,775,274 , GRCh38 chr7: 5,989,047-6,735,643 PMS2, RAC1, 22 more genes
    nsv5582253copy number variation1nstd207human GRCh38 chr7: 6,463,881-6,464,016 , GRCh37.p13 chr7: 6,503,512-6,503,647 KDELR2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554365sequence alteration1nstd206human GRCh38 chr7: 5,895,867-6,829,202 , GRCh37.p13 chr7: 5,935,498-6,868,833 , RAC1, 28 more genes
    nsv5472111copy number variation1nstd206human GRCh38 chr7: 6,468,474-6,469,404 , GRCh37.p13 chr7: 6,508,105-6,509,035 KDELR2
    nsv5467730copy number variation1nstd206human GRCh38 chr7: 6,452,959-6,459,994 , GRCh37.p13 chr7: 6,492,590-6,499,625 KDELR2
    nsv5413484mobile element insertion1nstd206human GRCh38 chr7: 6,476,838-6,476,889 , GRCh37.p13 chr7: 6,516,469-6,516,520 KDELR2
    nsv5409341mobile element insertion1nstd206human GRCh38 chr7: 6,480,708-6,480,752 , GRCh37.p13 chr7: 6,520,339-6,520,383 KDELR2
    nsv5370161translocation1nstd200human GRCh38 chr7: 6,459,433-6,459,433 , GRCh38 chr7: 6,459,356-6,459,356 , GRCh37.p13 chr7: 6,499,064-6,499,064 , GRCh37.p13 chr7: 6,498,987-6,498,987 KDELR2
    nsv5336550translocation1nstd200human GRCh37 chr7: 6,498,987-6,498,987 , GRCh37 chr7: 6,499,064-6,499,064 , GRCh38.p12 chr7: 6,459,356-6,459,356 , GRCh38.p12 chr7: 6,459,433-6,459,433 KDELR2
    nsv5319623copy number variation1nstd204human GRCh38.p13 chr7: 6,480,311-6,480,901 , GRCh37.p13 chr7: 6,519,942-6,520,532 KDELR2
    nsv5300401copy number variation1nstd204human GRCh38.p13 chr7: 6,454,386-6,464,498 , GRCh37.p13 chr7: 6,494,017-6,504,129 KDELR2
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