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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058860inversion1nstd229human GRCh38 chr20: 23,712,885-24,705,501 , GRCh37.p13 chr20: 23,693,522-24,686,137 RNU1-23P, LOC105372585, 16 more genes
    nsv7037094copy number variation1nstd229human GRCh38 chr20: 23,996,469-25,641,348 , GRCh37.p13 chr20: 23,977,106-25,621,984 CST7, LOC105372579, 28 more genes
    nsv7033999copy number variation1nstd229human GRCh38 chr20: 24,211,801-24,221,400 , GRCh37.p13 chr20: 24,192,437-24,202,036 LINC01721
    nsv7032011copy number variation1nstd229human GRCh38 chr20: 23,203,457-24,359,303 , GRCh37.p13 chr20: 23,184,094-24,339,939 CST9, RNU1-23P, 32 more genes
    nsv7029901copy number variation1nstd229human GRCh38 chr20: 23,522,540-24,257,872 , GRCh37.p13 chr20: 23,503,177-24,238,508 POM121L3P, CST4, 20 more genes
    nsv7025942copy number variation1nstd229human GRCh38 chr20: 23,664,614-24,244,066 , GRCh37.p13 chr20: 23,645,251-24,224,702 WAKMAR1, RNU1-23P, 14 more genes
    nsv6637732copy number variation1nstd102humanUncertain significance GRCh37 chr20: 23,142,478-24,824,349 , GRCh38.p12 chr20: 23,161,841-24,843,713 NAPB, POM121L3P, 37 more genes
    nsv6532512copy number variation1nstd223human GRCh38 chr20: 24,209,438-24,209,907 , GRCh37.p13 chr20: 24,190,074-24,190,543 LINC01721
    nsv6518276copy number variation1nstd223human GRCh38 chr20: 24,215,201-24,224,700 , GRCh37.p13 chr20: 24,195,837-24,205,336 LINC01721
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6227361copy number variation1nstd214human GRCh38 chr20: 24,219,811-24,219,912 , GRCh37.p13 chr20: 24,200,447-24,200,548 LINC01721
    nsv6210341copy number variation1nstd214human GRCh38 chr20: 24,208,097-24,208,160 , GRCh37.p13 chr20: 24,188,733-24,188,796 LINC01721
    nsv6134282copy number variation1nstd213human GRCh37 chr20: 24,150,000-24,310,001 , GRCh38.p12 chr20: 24,169,364-24,329,365 LINC01721, LOC105372577, 1 more genes
    nsv6134018copy number variation1nstd213human GRCh37 chr20: 23,950,000-25,300,001 , GRCh38.p12 chr20: 23,969,363-25,319,365 ENTPD6, PYGB, 23 more genes
    nsv6048107copy number variation1nstd212human GRCh38 chr20: 24,208,336-24,208,393 , GRCh37.p13 chr20: 24,188,972-24,189,029 LINC01721
    nsv6045455copy number variation1nstd212human GRCh38 chr20: 24,208,190-24,208,247 , GRCh37.p13 chr20: 24,188,826-24,188,883 LINC01721
    nsv6041493copy number variation1nstd212human GRCh38 chr20: 24,208,267-24,208,538 , GRCh37.p13 chr20: 24,188,903-24,189,174 LINC01721
    nsv5721299mobile element insertion2nstd211human GRCh38 chr20: 24,214,042-24,214,042 , GRCh37.p13 chr20: 24,194,678-24,194,678 LINC01721
    nsv5604070copy number variation1nstd207human GRCh38 chr20: 24,219,811-24,219,912 , GRCh37.p13 chr20: 24,200,447-24,200,548 LINC01721
    nsv5328909copy number variation1nstd204human GRCh38.p13 chr20: 24,204,805-24,205,652 , GRCh37.p13 chr20: 24,185,441-24,186,288 LINC01721
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