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Items: 1 to 20 of 494

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965724insertion1nstd209human GRCh38 chr4: 79,256,645-79,256,645 , GRCh37.p13 chr4: 80,177,799-80,177,799 NAA11, LINC01088
    nsv5957684insertion1nstd209human GRCh38 chr4: 79,244,636-79,244,636 , GRCh37.p13 chr4: 80,165,790-80,165,790 NAA11, LINC01088
    nsv5950933insertion1nstd209human GRCh38 chr4: 79,189,145-79,189,145 , GRCh37.p13 chr4: 80,110,299-80,110,299 LINC01088, NAA11
    nsv5904185copy number variation1nstd209human GRCh38 chr4: 79,162,975-79,163,377 , GRCh37.p13 chr4: 80,084,129-80,084,531 LINC01088, NAA11
    nsv5893221copy number variation1nstd209human GRCh38 chr4: 79,284,574-79,284,901 , GRCh37.p13 chr4: 80,205,728-80,206,055 LINC01088, NAA11
    nsv5715241mobile element insertion1nstd211human GRCh38 chr4: 79,268,433-79,268,433 , GRCh37.p13 chr4: 80,189,587-80,189,587 NAA11, LINC01088
    nsv5689878mobile element insertion1nstd211human GRCh38 chr4: 79,321,911-79,321,911 , GRCh37.p13 chr4: 80,243,065-80,243,065 NAA11
    nsv5604949insertion1nstd207human GRCh38 chr4: 79,167,132-79,167,132 , GRCh37.p13 chr4: 80,088,286-80,088,286 NAA11, LINC01088
    nsv5570216copy number variation1nstd207human GRCh38 chr4: 79,284,574-79,284,901 , GRCh37.p13 chr4: 80,205,728-80,206,055 NAA11, LINC01088
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5472173copy number variation1nstd206human GRCh38 chr4: 79,222,802-79,223,657 , GRCh37.p13 chr4: 80,143,956-80,144,811 LINC01088, NAA11
    nsv5466737copy number variation1nstd206human GRCh38 chr4: 79,220,252-79,220,345 , GRCh37.p13 chr4: 80,141,406-80,141,499 NAA11, LINC01088
    nsv5465735copy number variation1nstd206human GRCh38 chr4: 79,284,589-79,284,902 , GRCh37.p13 chr4: 80,205,743-80,206,056 LINC01088, NAA11
    nsv5406752mobile element insertion1nstd206human GRCh38 chr4: 79,321,911-79,321,962 , GRCh37.p13 chr4: 80,243,065-80,243,116 NAA11
    nsv5384726mobile element deletion2nstd186human GRCh37 chr4: 80,205,743-80,206,056 , GRCh38.p12 chr4: 79,284,589-79,284,902 LINC01088, NAA11
    nsv5367628translocation1nstd200human GRCh38 chr4: 79,178,256-79,178,256 , GRCh38 chr4: 79,184,370-79,184,370 , GRCh37.p13 chr4: 80,099,410-80,099,410 , GRCh37.p13 chr4: 80,105,524-80,105,524 NAA11, LINC01088
    nsv5346763translocation1nstd200human GRCh38 chr4: 79,252,196-79,252,196 , GRCh38 chr4: 79,251,908-79,251,908 , GRCh37.p13 chr4: 80,173,062-80,173,062 , GRCh37.p13 chr4: 80,173,350-80,173,350 LINC01088, NAA11
    nsv5236840copy number variation1nstd204human GRCh38.p13 chr4: 79,284,601-79,284,900 , GRCh37.p13 chr4: 80,205,755-80,206,054 NAA11, LINC01088
    nsv5232366copy number variation1nstd204human GRCh38.p13 chr4: 79,226,724-79,229,893 , GRCh37.p13 chr4: 80,147,878-80,151,047 NAA11, LINC01088
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