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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5674716mobile element insertion2nstd211human GRCh38 chr4: 73,596,224-73,596,224 , GRCh37.p13 chr4: 74,461,941-74,461,941 RASSF6
    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
    nsv5605955insertion1nstd207human GRCh38 chr4: 73,596,210-73,596,210 , GRCh37.p13 chr4: 74,461,927-74,461,927 RASSF6
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5468558copy number variation1nstd206human GRCh38 chr4: 73,616,267-73,618,302 , GRCh37.p13 chr4: 74,481,984-74,484,019 RASSF6
    nsv5465265copy number variation1nstd206human GRCh38 chr4: 73,609,884-73,613,875 , GRCh37.p13 chr4: 74,475,601-74,479,592 RASSF6
    nsv5454299copy number variation1nstd206human GRCh38 chr4: 73,567,818-73,581,388 , GRCh37.p13 chr4: 74,433,535-74,447,105 RASSF6
    nsv5406799mobile element insertion1nstd206human GRCh38 chr4: 73,596,224-73,596,275 , GRCh37.p13 chr4: 74,461,941-74,461,992 RASSF6
    nsv5346720translocation1nstd200human GRCh38 chr4: 73,602,958-73,602,958 , GRCh38 chr4: 73,603,016-73,603,016 , GRCh37.p13 chr4: 74,468,675-74,468,675 , GRCh37.p13 chr4: 74,468,733-74,468,733 RASSF6
    nsv5335862translocation1nstd200human GRCh37 chr4: 74,443,958-74,443,958 , GRCh37 chr4: 74,444,025-74,444,025 , GRCh38.p12 chr4: 73,578,241-73,578,241 , GRCh38.p12 chr4: 73,578,308-73,578,308 RASSF6
    nsv5091998mobile element insertion1nstd203human GRCh38 chr4: 73,596,210-73,596,224 , GRCh37.p13 chr4: 74,461,927-74,461,941 RASSF6
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922976copy number variation1nstd200human GRCh38 chr4: 73,620,961-73,624,822 , GRCh37.p13 chr4: 74,486,678-74,490,539 RASSF6
    nsv4922975copy number variation1nstd200human GRCh38 chr4: 73,609,884-73,613,875 , GRCh37.p13 chr4: 74,475,601-74,479,592 RASSF6
    nsv4922974copy number variation1nstd200human GRCh38 chr4: 73,583,473-73,588,738 , GRCh37.p13 chr4: 74,449,190-74,454,455 RASSF6
    nsv4922973copy number variation1nstd200human GRCh38 chr4: 73,578,241-73,578,308 , GRCh37.p13 chr4: 74,443,958-74,444,025 RASSF6
    nsv4922972copy number variation1nstd200human GRCh38 chr4: 73,569,323-73,579,139 , GRCh37.p13 chr4: 74,435,040-74,444,856 RASSF6
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800224copy number variation1nstd200human GRCh37 chr4: 74,486,678-74,490,539 , GRCh38.p12 chr4: 73,620,961-73,624,822 RASSF6
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