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Items: 1 to 20 of 228

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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
    nsv6777485copy number variation1nstd229human GRCh38 chr5: 15,612,012-15,612,496 , GRCh37.p13 chr5: 15,612,121-15,612,605 FBXL7, CTD-2350J17.1
    nsv6775039copy number variation1nstd229human GRCh38 chr5: 15,085,905-15,875,076 , GRCh37.p13 chr5: 15,086,014-15,875,185 LOC391741, MARK2P5, 5 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
    nsv6771172copy number variation1nstd229human GRCh38 chr5: 15,072,511-15,667,851 , GRCh37.p13 chr5: 15,072,620-15,667,960 MARK2P5, LINC02149, 4 more genes
    nsv6767954copy number variation1nstd229human GRCh38 chr5: 15,231,062-15,754,718 , GRCh37.p13 chr5: 15,231,171-15,754,827 LOC391741, LOC100270647, 4 more genes
    nsv6763823copy number variation1nstd229human GRCh38 chr5: 15,603,523-15,606,395 , GRCh37.p13 chr5: 15,603,632-15,606,504 FBXL7, CTD-2350J17.1
    nsv6763778copy number variation1nstd229human GRCh38 chr5: 15,603,660-15,606,389 , GRCh37.p13 chr5: 15,603,769-15,606,498 CTD-2350J17.1, FBXL7
    nsv6762682copy number variation1nstd229human GRCh38 chr5: 15,594,153-15,615,280 , GRCh37.p13 chr5: 15,594,262-15,615,389 FBXL7, CTD-2350J17.1
    nsv6760593copy number variation1nstd229human GRCh38 chr5: 15,606,429-15,617,238 , GRCh37.p13 chr5: 15,606,538-15,617,347 FBXL7, CTD-2350J17.1
    nsv6758848copy number variation1nstd229human GRCh38 chr5: 15,533,429-15,604,012 , GRCh37.p13 chr5: 15,533,538-15,604,121 CTD-2350J17.1, FBXL7
    nsv6758822copy number variation1nstd229human GRCh38 chr5: 15,604,470-15,604,663 , GRCh37.p13 chr5: 15,604,579-15,604,772 CTD-2350J17.1, FBXL7
    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
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