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Items: 1 to 20 of 151

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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
    nsv7002701copy number variation1nstd229human GRCh38 chr20: 1,321,105-1,325,354 , GRCh37.p13 chr20: 1,301,749-1,305,998 SDCBP2, FKBP1A-SDCBP2, 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
    nsv6532073copy number variation1nstd223human GRCh38 chr20: 1,321,104-1,325,354 , GRCh37.p13 chr20: 1,301,748-1,305,998 SDCBP2-AS1, SDCBP2, 1 more genes
    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
    nsv5515547copy number variation1nstd206human GRCh38 chr20: 1,327,149-1,337,203 , GRCh37.p13 chr20: 1,307,793-1,317,847 SDCBP2, SDCBP2-AS1, 1 more genes
    nsv5028341copy number variation1nstd200human GRCh38 chr20: 1,321,103-1,325,354 , GRCh37.p13 chr20: 1,301,747-1,305,998 SDCBP2, FKBP1A-SDCBP2, 1 more genes
    nsv5028340copy number variation1nstd200human GRCh38 chr20: 1,319,198-1,319,402 , GRCh37.p13 chr20: 1,299,842-1,300,046 FKBP1A-SDCBP2, SDCBP2
    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
    nsv4629434copy number variation1nstd183human GRCh37 chr20: 1,307,738-1,317,799 , GRCh38.p12 chr20: 1,327,094-1,337,155 SDCBP2, FKBP1A-SDCBP2, 1 more genes
    nsv4430172copy number variation1nstd174human GRCh37 chr20: 1,307,697-1,318,064 , GRCh38.p12 chr20: 1,327,053-1,337,420 SDCBP2, SDCBP2-AS1, 1 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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