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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7077895inversion1nstd229human GRCh38 chr20: 265,739-1,834,868 , GRCh37.p13 chr20: 246,380-1,815,514 PSMF1, LOC105372498, 46 more genes
    nsv7074650inversion1nstd229human GRCh38 chr20: 945,543-2,680,685 , GRCh37.p13 chr20: 926,186-2,661,331 , SDCBP2-AS1, 54 more genes
    nsv7012736copy number variation1nstd229human GRCh38 chr20: 1,007,152-1,456,181 , GRCh37.p13 chr20: 987,795-1,436,826 ACTG1P3, SDCBP2, 12 more genes
    nsv7006338copy number variation1nstd229human GRCh38 chr20: 843,247-1,354,687 , GRCh37.p13 chr20: 823,890-1,335,331 SDCBP2, FKBP1A-SDCBP2, 12 more genes
    nsv7004112copy number variation1nstd229human GRCh38 chr20: 997,301-1,207,268 , GRCh37.p13 chr20: 977,944-1,187,912 C20orf202, PSMF1, 4 more genes
    nsv7001310copy number variation1nstd229human GRCh38 chr20: 1,202,526-1,265,397 , GRCh37.p13 chr20: 1,183,170-1,246,041 SNPH, RAD21L1, 1 more genes
    nsv6637913copy number variation1nstd102humanUncertain significance GRCh37 chr20: 1,015,167-1,403,720 , GRCh38.p12 chr20: 1,034,524-1,423,076 FKBP1A, TMEM74B, 11 more genes
    nsv6637260copy number variation1nstd102humanUncertain significance GRCh37 chr20: 992,980-1,481,478 , GRCh38.p12 chr20: 1,012,337-1,500,832 TMEM74B, NSFL1C, 13 more genes
    nsv6626302copy number variation1nstd224human GRCh37 chr20: 1,002,656-1,187,586 , GRCh38.p12 chr20: 1,022,013-1,206,942 ACTG1P3, PSMF1, 3 more genes
    nsv6517777copy number variation1nstd223human GRCh38 chr20: 1,207,656-1,208,013 , GRCh37.p13 chr20: 1,188,300-1,188,657 C20orf202
    nsv6134008copy number variation1nstd213human GRCh37 chr20: 1,070,000-1,560,001 , GRCh38.p12 chr20: 1,089,357-1,579,355 ACTG1P3, SDCBP2, 19 more genes
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5196877mobile element insertion1nstd203human GRCh38 chr20: 1,208,240-1,208,256 , GRCh37.p13 chr20: 1,188,884-1,188,900 C20orf202
    nsv4676288copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327 TBC1D20, RAD21L1, 34 more genes
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4676163copy number variation1nstd102humanUncertain significance GRCh37 chr20: 989,820-1,216,980 , GRCh38.p12 chr20: 1,009,177-1,236,336 C20orf202, PSMF1, 4 more genes
    nsv4457692copy number variation1nstd102humanUncertain significance GRCh37 chr20: 728,577-1,237,670 , GRCh38.p12 chr20: 747,933-1,257,026 TMEM74B, RAD21L1, 10 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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