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Items: 1 to 20 of 173

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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
    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
    nsv6771926copy number variation1nstd229human GRCh38 chr5: 14,679,181-16,033,154 , GRCh37.p13 chr5: 14,679,290-16,033,263 MIR4637, LOC100270647, 18 more genes
    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
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6311748copy number variation2nstd102humanUncertain significance GRCh37 chr5: 13,692,093-14,871,567 , GRCh38.p12 chr5: 13,691,984-14,871,458 RBBP4P1, TRIO, 11 more genes
    nsv6291096copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-16,952,167 , GRCh38.p12 chr5: 113,462-16,952,058 MIR4457, HNRNPKP5, 222 more genes
    nsv6136143copy number variation1nstd213human GRCh37 chr5: 9,360,000-26,560,001 , GRCh38.p12 chr5: 9,359,888-26,559,892 FTH1P10, MYO10, 163 more genes
    nsv6135687copy number variation1nstd213human GRCh37 chr5: 9,400,000-26,970,001 , GRCh38.p12 chr5: 9,399,888-26,969,894 DNAH5, MSNP1, 165 more genes
    nsv6135644copy number variation1nstd213human GRCh37 chr5: 12,190,000-14,790,001 , GRCh38.p12 chr5: 12,189,888-14,789,892 OTULIN, CCT6P2, 21 more genes
    nsv6135382copy number variation1nstd213human GRCh37 chr5: 13,280,000-16,740,001 , GRCh38.p12 chr5: 13,279,888-16,739,892 MYO10, FBXL7, 39 more genes
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