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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070559inversion1nstd229human GRCh38 chr20: 31,426,398-31,479,070 , GRCh37.p13 chr20: 30,014,201-30,066,873 DEFB122, REM1, 2 more genes
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7037901copy number variation1nstd229human GRCh38 chr20: 31,423,301-31,739,500 , GRCh37.p13 chr20: 30,011,104-30,327,303 BCL2L1, DEFB123, 18 more genes
    nsv7032945copy number variation1nstd229human GRCh38 chr20: 31,283,144-31,615,397 , GRCh37.p13 chr20: 29,870,947-30,203,200 HM13-AS1, DEFB119, 22 more genes
    nsv7032549copy number variation1nstd229human GRCh38 chr20: 31,308,013-31,715,090 , GRCh37.p13 chr20: 29,895,816-30,302,893 TRS-AGA7-1, ID1, 24 more genes
    nsv7025136copy number variation1nstd229human GRCh38 chr20: 31,456,221-31,905,173 , GRCh37.p13 chr20: 30,044,024-30,492,976 COX4I2, CD24P3, 21 more genes
    nsv7024687copy number variation1nstd229human GRCh38 chr20: 31,439,651-31,493,591 , GRCh37.p13 chr20: 30,027,454-30,081,394 DEFB124, DEFB123, 2 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
    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
    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
    nsv6599127inversion1nstd223human GRCh38 chr20: 31,479,783-31,480,494 , GRCh37.p13 chr20: 30,067,586-30,068,297 REM1
    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
    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
    nsv5879352copy number variation1nstd209human GRCh38 chr20: 31,463,142-31,512,067 , GRCh37.p13 chr20: 30,050,945-30,099,870 REM1, LINC00028, 3 more genes
    nsv5323761copy number variation1nstd204human GRCh37.p13 chr20: 30,060,631-30,164,744 , GRCh38.p13 chr20: 31,472,828-31,576,941 CD24P3, REM1, 7 more genes
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