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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076785inversion1nstd229human GRCh38 chr20: 36,001,722-37,069,571 , GRCh37.p13 chr20: 34,589,644-35,697,974 RPS3AP3, EPB41L1-AS1, 22 more genes
    nsv7033746copy number variation1nstd229human GRCh38 chr20: 36,576,326-36,581,371 , GRCh37.p13 chr20: 35,204,729-35,209,774 TGIF2, TGIF2-RAB5IF
    nsv7028183copy number variation1nstd229human GRCh38 chr20: 36,588,755-36,598,163 , GRCh37.p13 chr20: 35,217,158-35,226,566 TGIF2, TGIF2-RAB5IF
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020388copy number variation1nstd229human GRCh38 chr20: 36,573,175-36,583,842 , GRCh37.p13 chr20: 35,201,578-35,212,245 TGIF2-RAB5IF, TGIF2, 1 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6134023copy number variation1nstd213human GRCh37 chr20: 34,270,000-35,840,001 , GRCh38.p12 chr20: 35,682,078-37,211,598 RBL1, AAR2, 35 more genes
    nsv6042135copy number variation1nstd212human GRCh38 chr20: 36,583,542-36,583,678 , GRCh37.p13 chr20: 35,211,945-35,212,081 TGIF2, TGIF2-RAB5IF
    nsv5560305sequence alteration1nstd206human GRCh38 chr20: 36,507,286-36,660,208 , GRCh37.p13 chr20: 35,135,689-35,288,611 , MYL9, 8 more genes
    nsv5523028copy number variation1nstd206human GRCh38 chr20: 36,593,418-36,593,717 , GRCh37.p13 chr20: 35,221,821-35,222,120 TGIF2, TGIF2-RAB5IF
    nsv5028490copy number variation1nstd200human GRCh38 chr20: 36,580,888-36,583,017 , GRCh37.p13 chr20: 35,209,291-35,211,420 TGIF2, TGIF2-RAB5IF
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4290827copy number variation1nstd166human GRCh37.p13 chr20: 35,221,282-35,222,572 , GRCh38.p12 chr20: 36,592,879-36,594,169 TGIF2, TGIF2-RAB5IF
    nsv4275780copy number variation1nstd166human GRCh37.p13 chr20: 35,211,543-35,215,261 , GRCh38.p12 chr20: 36,583,140-36,586,858 TGIF2-RAB5IF, TGIF2
    nsv4273255copy number variation1nstd166human GRCh37.p13 chr20: 35,208,090-35,208,207 , GRCh38.p12 chr20: 36,579,687-36,579,804 TGIF2-RAB5IF, TGIF2
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