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Items: 1 to 20 of 294

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047334inversion1nstd229human GRCh38 chr5: 119,494,072-128,765,801 , GRCh37.p13 chr5: 118,829,767-128,101,494 RPL18P3, KRT18P16, 98 more genes
    nsv6777725copy number variation1nstd229human GRCh38 chr5: 123,275,548-123,574,881 , GRCh37.p13 chr5: 122,611,242-122,910,575 HMGB3P17, KRT8P33, 2 more genes
    nsv6772733copy number variation1nstd229human GRCh38 chr5: 123,598,201-123,680,900 , GRCh37.p13 chr5: 122,933,895-123,016,594 KRT18P16, CSNK1G3
    nsv6771130copy number variation1nstd229human GRCh38 chr5: 123,577,679-123,584,030 , GRCh37.p13 chr5: 122,913,373-122,919,724 CSNK1G3
    nsv6769822copy number variation1nstd229human GRCh38 chr5: 123,575,963-123,588,065 , GRCh37.p13 chr5: 122,911,657-122,923,759 CSNK1G3
    nsv6768880copy number variation1nstd229human GRCh38 chr5: 123,519,091-123,527,162 , GRCh37.p13 chr5: 122,854,785-122,862,856 CSNK1G3
    nsv6768106copy number variation1nstd229human GRCh38 chr5: 123,605,453-123,605,958 , GRCh37.p13 chr5: 122,941,147-122,941,652 CSNK1G3
    nsv6765661copy number variation1nstd229human GRCh38 chr5: 123,596,461-123,596,544 , GRCh37.p13 chr5: 122,932,155-122,932,238 CSNK1G3
    nsv6764322copy number variation1nstd229human GRCh38 chr5: 123,322,839-124,149,356 , GRCh37.p13 chr5: 122,658,533-123,485,049 KRT8P33, LINC01170, 5 more genes
    nsv6761298copy number variation1nstd229human GRCh38 chr5: 123,522,601-123,526,700 , GRCh37.p13 chr5: 122,858,295-122,862,394 CSNK1G3
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6636228copy number variation1nstd102humanUncertain significance GRCh37 chr5: 122,610,315-122,912,616 , GRCh38.p12 chr5: 123,274,621-123,576,922 KRT8P33, HMGB3P17, 2 more genes
    nsv6570806inversion1nstd223human GRCh38 chr5: 123,574,000-123,574,583 , GRCh37.p13 chr5: 122,909,694-122,910,277 CSNK1G3
    nsv6557060inversion1nstd223human GRCh38 chr5: 123,560,124-123,560,205 , GRCh37.p13 chr5: 122,895,818-122,895,899 CSNK1G3
    nsv6415223copy number variation1nstd223human GRCh38 chr5: 123,576,331-123,576,912 , GRCh37.p13 chr5: 122,912,025-122,912,606 CSNK1G3
    nsv6414875copy number variation1nstd223human GRCh38 chr5: 123,531,501-123,534,000 , GRCh37.p13 chr5: 122,867,195-122,869,694 CSNK1G3
    nsv6413432copy number variation1nstd223human GRCh38 chr5: 123,518,143-123,518,680 , GRCh37.p13 chr5: 122,853,837-122,854,374 CSNK1G3
    nsv6412526copy number variation1nstd223human GRCh38 chr5: 123,589,901-123,591,000 , GRCh37.p13 chr5: 122,925,595-122,926,694 CSNK1G3
    nsv6411422copy number variation1nstd223human GRCh38 chr5: 123,597,139-123,597,717 , GRCh37.p13 chr5: 122,932,833-122,933,411 CSNK1G3
    nsv6400852copy number variation1nstd223human GRCh38 chr5: 123,591,686-123,592,218 , GRCh37.p13 chr5: 122,927,380-122,927,912 CSNK1G3
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