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Items: 1 to 20 of 1725

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7147532insertion1nstd232human GRCh37.p13 chr4: 81,456,499-81,456,499 , GRCh38.p12 chr4: 80,535,345-80,535,345 CFAP299
    nsv7137509copy number variation1nstd232human GRCh37.p13 chr4: 81,823,590-81,823,645 , GRCh38.p12 chr4: 80,902,436-80,902,491 CFAP299
    nsv7055488inversion1nstd229human GRCh38 chr4: 80,396,198-80,396,272 , GRCh37.p13 chr4: 81,317,352-81,317,426 CFAP299
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7052914inversion1nstd229human GRCh38 chr4: 80,960,607-80,966,599 , GRCh37.p13 chr4: 81,881,761-81,887,753 CFAP299
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7048659inversion1nstd229human GRCh38 chr4: 80,779,464-80,781,683 , GRCh37.p13 chr4: 81,700,618-81,702,837 CFAP299
    nsv7048249inversion1nstd229human GRCh38 chr4: 80,951,351-80,977,877 , GRCh37.p13 chr4: 81,872,505-81,899,031 CFAP299
    nsv7046327inversion1nstd229human GRCh38 chr4: 80,434,032-80,434,065 , GRCh37.p13 chr4: 81,355,186-81,355,219 CFAP299
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv7040401inversion1nstd229human GRCh38 chr4: 80,786,021-80,805,843 , GRCh37.p13 chr4: 81,707,175-81,726,997 CFAP299
    nsv7039298inversion1nstd229human GRCh38 chr4: 80,906,035-81,079,164 , GRCh37.p13 chr4: 81,827,189-82,000,318 BMP3, CFAP299
    nsv6757938copy number variation1nstd229human GRCh38 chr4: 80,904,538-80,908,667 , GRCh37.p13 chr4: 81,825,692-81,829,821 CFAP299
    nsv6757744copy number variation1nstd229human GRCh38 chr4: 80,476,750-80,477,510 , GRCh37.p13 chr4: 81,397,904-81,398,664 CFAP299
    nsv6757456copy number variation1nstd229human GRCh38 chr4: 80,501,040-80,501,798 , GRCh37.p13 chr4: 81,422,194-81,422,952 CFAP299
    nsv6757443copy number variation1nstd229human GRCh38 chr4: 80,384,116-80,429,081 , GRCh37.p13 chr4: 81,305,270-81,350,235 LOC100419739, CFAP299
    nsv6757057copy number variation1nstd229human GRCh38 chr4: 80,371,652-80,389,829 , GRCh37.p13 chr4: 81,292,806-81,310,983 LOC100419739, CFAP299
    nsv6756941copy number variation1nstd229human GRCh38 chr4: 80,325,296-80,340,482 , GRCh37.p13 chr4: 81,246,450-81,261,636 CFAP299
    nsv6756452copy number variation1nstd229human GRCh38 chr4: 80,367,501-80,378,200 , GRCh37.p13 chr4: 81,288,655-81,299,354 CFAP299
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