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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098841copy number variation1nstd102humanPathogenic GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191 RN7SKP133, TAF11L1, 102 more genes
    nsv7053949inversion1nstd229human GRCh38 chr5: 12,599,104-19,642,739 , GRCh37.p13 chr5: 12,599,216-19,642,848 H3P18, H3P19, 86 more genes
    nsv7050365inversion1nstd229human GRCh38 chr5: 14,584,216-14,584,287 , GRCh37.p13 chr5: 14,584,325-14,584,396 OTULINL
    nsv7049801inversion1nstd229human GRCh38 chr5: 13,579,109-16,991,898 , GRCh37.p13 chr5: 13,579,218-16,992,007 MARCHF11-DT, OTULIN, 41 more genes
    nsv7038921inversion1nstd229human GRCh38 chr5: 14,117,099-14,986,488 , GRCh37.p13 chr5: 14,117,208-14,986,597 OTULINL, UQCRBP3, 15 more genes
    nsv7038701inversion1nstd229human GRCh38 chr5: 12,558,868-18,815,622 , GRCh37.p13 chr5: 12,558,980-18,815,731 FBXL7, LINC02223, 81 more genes
    nsv6768952copy number variation1nstd229human GRCh38 chr5: 14,613,201-14,618,900 , GRCh37.p13 chr5: 14,613,310-14,619,009 LOC100422687, OTULINL
    nsv6765961copy number variation1nstd229human GRCh38 chr5: 14,570,159-14,586,908 , GRCh37.p13 chr5: 14,570,268-14,587,017 OTULINL
    nsv6765537copy number variation1nstd229human GRCh38 chr5: 14,600,820-14,614,512 , GRCh37.p13 chr5: 14,600,929-14,614,621 OTULINL
    nsv6760127copy number variation1nstd229human GRCh38 chr5: 14,574,490-14,583,057 , GRCh37.p13 chr5: 14,574,599-14,583,166 OTULINL
    nsv6759092copy number variation1nstd229human GRCh38 chr5: 14,589,017-14,591,793 , GRCh37.p13 chr5: 14,589,126-14,591,902 OTULINL
    nsv6758179copy number variation1nstd229human GRCh38 chr5: 14,609,188-14,616,198 , GRCh37.p13 chr5: 14,609,297-14,616,307 OTULINL
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6394264copy number variation1nstd223human GRCh38 chr5: 14,236,796-14,758,136 , GRCh37.p13 chr5: 14,236,905-14,758,245 EEF1A1P13, OTULINL, 8 more genes
    nsv6388088copy number variation1nstd223human GRCh38 chr5: 14,591,145-14,592,566 , GRCh37.p13 chr5: 14,591,254-14,592,675 OTULINL
    nsv6382251copy number variation1nstd223human GRCh38 chr5: 14,574,490-14,583,054 , GRCh37.p13 chr5: 14,574,599-14,583,163 OTULINL
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