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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050610inversion1nstd229human GRCh38 chr5: 31,546,108-31,546,225 , GRCh37.p13 chr5: 31,546,215-31,546,332 C5orf22
    nsv6771811copy number variation1nstd229human GRCh38 chr5: 31,333,856-32,197,880 , GRCh37.p13 chr5: 31,333,963-32,197,986 GOLPH3, MIR4279, 12 more genes
    nsv6770066copy number variation1nstd229human GRCh38 chr5: 31,527,215-31,530,568 , GRCh37.p13 chr5: 31,527,322-31,530,675 C5orf22, DROSHA
    nsv6765419copy number variation1nstd229human GRCh38 chr5: 31,525,752-31,537,925 , GRCh37.p13 chr5: 31,525,859-31,538,032 C5orf22, DROSHA
    nsv6761647copy number variation1nstd229human GRCh38 chr5: 31,082,736-31,663,838 , GRCh37.p13 chr5: 31,082,843-31,663,945 C5orf22, DROSHA, 5 more genes
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6562317inversion1nstd223human GRCh38 chr5: 31,544,497-31,545,162 , GRCh37.p13 chr5: 31,544,604-31,545,269 C5orf22
    nsv6394921copy number variation1nstd223human GRCh38 chr5: 31,548,450-31,550,257 , GRCh37.p13 chr5: 31,548,557-31,550,364 C5orf22
    nsv6391667copy number variation1nstd223human GRCh38 chr5: 31,555,201-31,558,400 , GRCh37.p13 chr5: 31,555,308-31,558,507 C5orf22
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6296383copy number variation1nstd186human GRCh37 chr5: 31,533,496-31,533,565 , GRCh38.p12 chr5: 31,533,389-31,533,458 C5orf22
    nsv6135406copy number variation1nstd213human GRCh37 chr5: 31,280,000-36,080,001 , GRCh38.p12 chr5: 31,279,893-36,079,899 IL7R, NPR3, 64 more genes
    nsv6135175copy number variation1nstd213human GRCh37 chr5: 29,210,000-46,400,001 , GRCh38.p12 chr5: 29,209,893-46,399,899 CDH6, HMGCS1, 210 more genes
    nsv5582123copy number variation1nstd207human GRCh38 chr5: 31,533,388-31,533,457 , GRCh37.p13 chr5: 31,533,495-31,533,564 C5orf22
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5470791copy number variation1nstd206human GRCh38 chr5: 31,555,455-31,558,138 , GRCh37.p13 chr5: 31,555,562-31,558,245 C5orf22
    nsv5465585copy number variation1nstd206human GRCh38 chr5: 31,555,398-31,558,010 , GRCh37.p13 chr5: 31,555,505-31,558,117 C5orf22
    nsv5463907copy number variation1nstd206human GRCh38 chr5: 31,533,389-31,533,458 , GRCh37.p13 chr5: 31,533,496-31,533,565 C5orf22
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