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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097148copy number variation1nstd102humanPathogenic GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680 RPL37P25, CCNO, 69 more genes
    nsv7057901inversion1nstd229human GRCh38 chr5: 53,201,194-56,162,991 , GRCh37.p13 chr5: 52,497,024-55,458,818 , PLPP1, 55 more genes
    nsv7056130inversion1nstd229human GRCh38 chr5: 53,218,622-56,162,980 , GRCh37.p13 chr5: 52,514,452-55,458,807 , ASS1P9, 54 more genes
    nsv7051847inversion1nstd229human GRCh38 chr5: 55,137,972-55,138,007 , GRCh37.p13 chr5: 54,433,800-54,433,835 CDC20B
    nsv6776074copy number variation1nstd229human GRCh38 chr5: 55,134,599-55,137,657 , GRCh37.p13 chr5: 54,430,427-54,433,485 CDC20B
    nsv6775540copy number variation1nstd229human GRCh38 chr5: 55,109,363-55,116,899 , GRCh37.p13 chr5: 54,405,191-54,412,727 CDC20B, GZMA
    nsv6775205copy number variation1nstd229human GRCh38 chr5: 55,150,737-55,155,421 , GRCh37.p13 chr5: 54,446,565-54,451,249 CDC20B
    nsv6774075copy number variation1nstd229human GRCh38 chr5: 55,072,701-55,112,100 , GRCh37.p13 chr5: 54,368,529-54,407,928 GZMA, CDC20B, 1 more genes
    nsv6773978copy number variation1nstd229human GRCh38 chr5: 55,134,042-55,139,865 , GRCh37.p13 chr5: 54,429,870-54,435,693 CDC20B
    nsv6771239copy number variation1nstd229human GRCh38 chr5: 55,148,501-55,152,900 , GRCh37.p13 chr5: 54,444,329-54,448,728 CDC20B
    nsv6768878copy number variation1nstd229human GRCh38 chr5: 55,127,618-55,156,431 , GRCh37.p13 chr5: 54,423,446-54,452,259 CDC20B
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6560545inversion1nstd223human GRCh38 chr5: 55,171,263-55,171,614 , GRCh37.p13 chr5: 54,467,091-54,467,442 MIR449C, CDC20B
    nsv6412724copy number variation1nstd223human GRCh38 chr5: 55,167,201-55,178,300 , GRCh37.p13 chr5: 54,463,029-54,474,128 CDC20B, GPX8, 3 more genes
    nsv6410305copy number variation1nstd223human GRCh38 chr5: 55,149,401-55,150,200 , GRCh37.p13 chr5: 54,445,229-54,446,028 CDC20B
    nsv6407236copy number variation1nstd223human GRCh38 chr5: 55,161,701-55,260,700 , GRCh37.p13 chr5: 54,457,529-54,556,528 CCNO, DHX29, 6 more genes
    nsv6401693copy number variation1nstd223human GRCh38 chr5: 55,116,904-55,121,346 , GRCh37.p13 chr5: 54,412,732-54,417,174 CDC20B
    nsv6401083copy number variation1nstd223human GRCh38 chr5: 55,119,185-55,119,797 , GRCh37.p13 chr5: 54,415,013-54,415,625 CDC20B
    nsv6399526copy number variation1nstd223human GRCh38 chr5: 55,169,801-55,186,300 , GRCh37.p13 chr5: 54,465,629-54,482,128 MIR449B, MIR449A, 2 more genes
    nsv6260336mobile element insertion1nstd215human GRCh38 chr5: 55,139,569-55,139,569 , GRCh37.p13 chr5: 54,435,397-54,435,397 CDC20B
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