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Items: 1 to 20 of 334

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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
    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
    nsv6770145copy number variation1nstd229human GRCh38 chr5: 6,306,635-6,311,738 , GRCh37.p13 chr5: 6,306,748-6,311,851 LINC02145
    nsv6766492copy number variation1nstd229human GRCh38 chr5: 6,325,795-6,335,843 , GRCh37.p13 chr5: 6,325,908-6,335,956 LINC02145
    nsv6766007copy number variation1nstd229human GRCh38 chr5: 6,319,252-6,320,146 , GRCh37.p13 chr5: 6,319,365-6,320,259 LINC02145
    nsv6764191copy number variation1nstd229human GRCh38 chr5: 6,295,901-6,328,200 , GRCh37.p13 chr5: 6,296,014-6,328,313 LINC02145
    nsv6764014copy number variation1nstd229human GRCh38 chr5: 6,301,160-6,311,375 , GRCh37.p13 chr5: 6,301,273-6,311,488 LINC02145
    nsv6762084copy number variation1nstd229human GRCh38 chr5: 6,231,049-7,367,961 , GRCh37.p13 chr5: 6,231,162-7,368,074 SRD5A1, LOC100130063, 23 more genes
    nsv6760175copy number variation1nstd229human GRCh38 chr5: 6,314,771-6,314,836 , GRCh37.p13 chr5: 6,314,884-6,314,949 LINC02145
    nsv6758673copy number variation1nstd229human GRCh38 chr5: 6,307,439-6,428,223 , GRCh37.p13 chr5: 6,307,552-6,428,336 MED10, LINC02145
    nsv6758375copy number variation1nstd229human GRCh38 chr5: 6,253,745-6,339,866 , GRCh37.p13 chr5: 6,253,858-6,339,979 HMGB3P3, LINC02145
    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
    nsv6630783copy number variation1nstd224human GRCh37 chr5: 6,266,723-6,336,397 , GRCh38.p12 chr5: 6,266,610-6,336,284 LINC02145, HMGB3P3
    nsv6630363copy number variation1nstd224human GRCh37 chr5: 6,336,397-6,358,449 , GRCh38.p12 chr5: 6,336,284-6,358,336 LINC02145
    nsv6630362copy number variation1nstd224human GRCh37 chr5: 6,296,147-6,340,693 , GRCh38.p12 chr5: 6,296,034-6,340,580 LINC02145
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