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Items: 1 to 20 of 257

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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
    nsv7038701inversion1nstd229human GRCh38 chr5: 12,558,868-18,815,622 , GRCh37.p13 chr5: 12,558,980-18,815,731 FBXL7, LINC02223, 81 more genes
    nsv6776646copy number variation1nstd229human GRCh38 chr5: 15,978,948-16,585,261 , GRCh37.p13 chr5: 15,979,057-16,585,370 MARCHF11, MARCHF11-AS1, 8 more genes
    nsv6772634copy number variation1nstd229human GRCh38 chr5: 16,173,101-16,230,200 , GRCh37.p13 chr5: 16,173,210-16,230,309 MARCHF11-DT, NACAP6, 2 more genes
    nsv6770029copy number variation1nstd229human GRCh38 chr5: 16,184,384-16,275,599 , GRCh37.p13 chr5: 16,184,493-16,275,708 MARCHF11-DT, NACAP6
    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
    nsv6385929copy number variation1nstd223human GRCh38 chr5: 16,174,701-16,183,200 , GRCh37.p13 chr5: 16,174,810-16,183,309 LOC105379640, MARCHF11-DT, 1 more genes
    nsv6381005copy number variation1nstd223human GRCh38 chr5: 16,113,562-16,252,752 , GRCh37.p13 chr5: 16,113,671-16,252,861 MARCHF11-AS1, MARCHF11, 3 more genes
    nsv6379987copy number variation1nstd223human GRCh38 chr5: 16,176,801-16,180,000 , GRCh37.p13 chr5: 16,176,910-16,180,109 LOC105379640, MARCHF11-DT, 1 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
    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
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