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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7029357copy number variation1nstd229human GRCh38 chr20: 32,596,820-32,597,200 , GRCh37.p13 chr20: 31,184,622-31,185,002 NOL4L-DT
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7025047copy number variation1nstd229human GRCh38 chr20: 32,604,363-32,607,509 , GRCh37.p13 chr20: 31,192,165-31,195,311 NOL4L-DT
    nsv7024903copy number variation1nstd229human GRCh38 chr20: 32,591,377-32,591,503 , GRCh37.p13 chr20: 31,179,179-31,179,305 NOL4L-DT
    nsv7020142copy number variation1nstd229human GRCh38 chr20: 32,598,396-32,598,577 , GRCh37.p13 chr20: 31,186,198-31,186,379 NOL4L-DT
    nsv7019507copy number variation1nstd229human GRCh38 chr20: 32,597,001-32,601,500 , GRCh37.p13 chr20: 31,184,803-31,189,302 NOL4L-DT
    nsv7018773copy number variation1nstd229human GRCh38 chr20: 32,518,401-32,743,500 , GRCh37.p13 chr20: 31,106,204-31,331,306 C20orf203, LOC101929698, 5 more genes
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 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
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 more genes
    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
    nsv6133806copy number variation1nstd213human GRCh37 chr20: 30,990,000-32,330,001 , GRCh38.p12 chr20: 32,402,197-33,742,195 SNTA1, ZNF341, 36 more genes
    nsv5523566copy number variation1nstd206human GRCh38 chr20: 32,588,675-32,588,984 , GRCh37.p13 chr20: 31,176,477-31,176,786 NOL4L-DT
    nsv5514050copy number variation1nstd206human GRCh38 chr20: 32,591,377-32,591,504 , GRCh37.p13 chr20: 31,179,179-31,179,306 NOL4L-DT
    nsv5165647mobile element insertion1nstd203human GRCh38 chr20: 32,608,859-32,608,874 , GRCh37.p13 chr20: 31,196,661-31,196,676 NOL4L-DT
    nsv5025512copy number variation1nstd200human GRCh38 chr20: 32,590,686-32,592,708 , GRCh37.p13 chr20: 31,178,488-31,180,510 NOL4L-DT
    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
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