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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7053901inversion1nstd229human GRCh38 chr5: 3,129,013-8,027,353 , GRCh37.p13 chr5: 3,129,127-8,027,466 FASTKD3, LOC101929200, 58 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv7042270inversion1nstd229human GRCh38 chr5: 4,344,295-6,275,858 , GRCh37.p13 chr5: 4,344,408-6,275,971 LOC105374629, MTCO2P30, 15 more genes
    nsv7041014inversion1nstd229human GRCh38 chr5: 5,430,959-5,433,309 , GRCh37.p13 chr5: 5,431,072-5,433,422 ICE1
    nsv7040546inversion1nstd229human GRCh38 chr5: 4,326,347-6,141,150 , GRCh37.p13 chr5: 4,326,460-6,141,263 LOC105374634, MTCO1P31, 15 more genes
    nsv6777516copy number variation1nstd229human GRCh38 chr5: 5,471,975-5,472,122 , GRCh37.p13 chr5: 5,472,088-5,472,235 ICE1
    nsv6774652copy number variation1nstd229human GRCh38 chr5: 4,946,640-6,484,597 , GRCh37.p13 chr5: 4,946,753-6,484,710 RN7SKP73, LINC01020, 17 more genes
    nsv6773158copy number variation1nstd229human GRCh38 chr5: 5,427,673-5,432,867 , GRCh37.p13 chr5: 5,427,786-5,432,980 ICE1
    nsv6770345copy number variation1nstd229human GRCh38 chr5: 5,456,601-5,615,200 , GRCh37.p13 chr5: 5,456,714-5,615,313 ICE1
    nsv6765199copy number variation1nstd229human GRCh38 chr5: 5,093,729-5,718,574 , GRCh37.p13 chr5: 5,093,842-5,718,687 MTCO1P30, ADAMTS16, 8 more genes
    nsv6764247copy number variation1nstd229human GRCh38 chr5: 5,467,754-5,468,144 , GRCh37.p13 chr5: 5,467,867-5,468,257 ICE1
    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
    nsv6574354inversion1nstd223human GRCh38 chr5: 2,721,509-7,652,209 , GRCh37.p13 chr5: 2,721,623-7,652,322 MIR4278, LOC442132, 60 more genes
    nsv6394553copy number variation1nstd223human GRCh38 chr5: 5,428,014-5,428,794 , GRCh37.p13 chr5: 5,428,127-5,428,907 ICE1
    nsv6384029copy number variation1nstd223human GRCh38 chr5: 5,451,048-5,451,555 , GRCh37.p13 chr5: 5,451,161-5,451,668 ICE1
    nsv6382930copy number variation1nstd223human GRCh38 chr5: 5,472,456-5,472,988 , GRCh37.p13 chr5: 5,472,569-5,473,101 ICE1
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