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Items: 1 to 20 of 208

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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
    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
    nsv6626563copy number variation1nstd224human GRCh37 chr20: 29,847,314-29,913,233 , GRCh38.p12 chr20: 31,259,511-31,325,430 RPL31P3, DEFB116, 3 more genes
    nsv6626562copy number variation1nstd224human GRCh37 chr20: 29,811,475-30,242,490 , GRCh38.p12 chr20: 31,223,672-31,654,687 CD24P3, DKKL1P1, 25 more genes
    nsv6626561copy number variation1nstd224human GRCh37 chr20: 29,811,475-29,858,213 , GRCh38.p12 chr20: 31,223,672-31,270,410 DEFB115
    nsv6626339copy number variation2nstd224human GRCh37 chr20: 29,833,609-30,070,197 , GRCh38.p12 chr20: 31,245,806-31,482,394 REM1, DEFB118, 13 more genes
    nsv6626338copy number variation1nstd224human GRCh37 chr20: 29,833,609-29,913,233 , GRCh38.p12 chr20: 31,245,806-31,325,430 DEFB116, DKKL1P1, 3 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
    nsv6291672copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,652,122-30,272,637 , GRCh38.p12 chr20: 30,417,446-31,684,834 DEFB124, LOC105379481, 47 more genes
    nsv6291590copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,652,122-30,518,304 , GRCh38.p12 chr20: 30,417,446-31,930,501 CDC27P4, DEFB122, 54 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
    nsv6291530copy number variation1nstd102humanLikely benign GRCh37 chr20: 29,833,535-30,195,919 , GRCh38.p12 chr20: 31,245,732-31,608,116 DEFB124, DEFB121, 24 more genes
    nsv6134283copy number variation1nstd213human GRCh37 chr20: 29,810,000-30,060,001 , GRCh38.p12 chr20: 31,222,197-31,472,198 DEFB121, DEFB124, 12 more genes
    nsv6133804copy number variation1nstd213human GRCh37 chr20: 29,500,000-30,240,001 , GRCh38.p12 chr20: 30,265,324-31,652,198 CD24P3, HM13, 50 more genes
    nsv5878681copy number variation1nstd209human GRCh38 chr20: 31,245,533-31,257,002 , GRCh37.p13 chr20: 29,833,336-29,844,805 DEFB115
    nsv5531179copy number variation1nstd206human GRCh38 chr20: 31,201,625-31,354,000 , GRCh37.p13 chr20: 29,803,910-29,941,803 DKKL1P1, RPL31P3, 4 more genes
    nsv5295628copy number variation1nstd204human GRCh38.p13 chr20: 31,251,633-31,266,132 , GRCh37.p13 chr20: 29,839,436-29,853,935 DEFB115
    nsv5283549copy number variation1nstd204human GRCh38.p13 chr20: 31,227,801-32,548,400 , GRCh37.p13 chr20: 29,815,604-31,136,202 , XKR7, 52 more genes
    nsv5280667copy number variation1nstd204human GRCh38.p13 chr20: 31,245,133-31,262,494 , GRCh37.p13 chr20: 29,832,936-29,850,297 DEFB115
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