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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
    nsv7068351inversion1nstd229human GRCh38 chr20: 1,449,115-1,449,165 , GRCh37.p13 chr20: 1,429,760-1,429,810 NSFL1C
    nsv7015334copy number variation1nstd229human GRCh38 chr20: 1,440,874-1,461,903 , GRCh37.p13 chr20: 1,421,519-1,442,548 NSFL1C
    nsv7012736copy number variation1nstd229human GRCh38 chr20: 1,007,152-1,456,181 , GRCh37.p13 chr20: 987,795-1,436,826 ACTG1P3, SDCBP2, 12 more genes
    nsv7008037copy number variation1nstd229human GRCh38 chr20: 1,443,734-1,449,429 , GRCh37.p13 chr20: 1,424,379-1,430,074 NSFL1C
    nsv7004708copy number variation1nstd229human GRCh38 chr20: 1,468,227-1,478,790 , GRCh37.p13 chr20: 1,448,872-1,459,435 SIRPB2, NSFL1C
    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
    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
    nsv5944128copy number variation1nstd209human GRCh38 chr20: 1,461,069-1,461,233 , GRCh37.p13 chr20: 1,441,714-1,441,878 NSFL1C
    nsv5695424mobile element insertion1nstd211human GRCh38 chr20: 1,458,581-1,458,581 , GRCh37.p13 chr20: 1,439,226-1,439,226 NSFL1C
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5283974copy number variation1nstd204human GRCh38.p13 chr20: 1,457,628-1,458,627 , GRCh37.p13 chr20: 1,438,273-1,439,272 NSFL1C
    nsv5173185mobile element insertion1nstd203human GRCh38 chr20: 1,449,176-1,449,189 , GRCh37.p13 chr20: 1,429,821-1,429,834 NSFL1C
    nsv4676270copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131 LOC100289473, STK35, 60 more genes
    nsv4630626copy number variation1nstd183human GRCh37 chr20: 1,387,340-2,110,072 , GRCh38.p12 chr20: 1,406,696-2,129,426 , STK35, 22 more genes
    nsv4567224insertion1nstd166human GRCh37.p13 chr20: 1,428,698-1,428,698 , GRCh38.p12 chr20: 1,448,053-1,448,053 NSFL1C
    nsv4511961mobile element insertion1nstd166human GRCh37.p13 chr20: 1,439,215-1,439,215 , GRCh38.p12 chr20: 1,458,570-1,458,570 NSFL1C
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