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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941659copy number variation1nstd209human GRCh38 chr20: 18,493,142-18,493,911 , GRCh37.p13 chr20: 18,473,786-18,474,555 RBBP9
    nsv5695271mobile element insertion2nstd211human GRCh38 chr20: 18,491,627-18,491,627 , GRCh37.p13 chr20: 18,472,271-18,472,271 RBBP9
    nsv5670756insertion1nstd207human GRCh38 chr20: 18,491,612-18,491,612 , GRCh37.p13 chr20: 18,472,256-18,472,256 RBBP9
    nsv5664832insertion1nstd207human GRCh38 chr20: 18,486,151-18,486,151 , GRCh37.p13 chr20: 18,466,795-18,466,795 RPL21P3, RBBP9
    nsv5590502copy number variation1nstd207human GRCh38 chr20: 18,486,127-18,486,188 , GRCh37.p13 chr20: 18,466,771-18,466,832 RPL21P3, RBBP9
    nsv5528671copy number variation1nstd206human GRCh38 chr20: 18,481,404-18,486,402 , GRCh37.p13 chr20: 18,462,048-18,467,046 POLR3F, RBBP9, 1 more genes
    nsv5414360mobile element insertion1nstd206human GRCh38 chr20: 18,491,627-18,491,678 , GRCh37.p13 chr20: 18,472,271-18,472,322 RBBP9
    nsv5165166mobile element insertion1nstd203human GRCh38 chr20: 18,491,612-18,491,627 , GRCh37.p13 chr20: 18,472,256-18,472,271 RBBP9
    nsv4680344copy number variation1nstd189human GRCh37.p13 chr20: 18,175,953-18,491,407 , GRCh38.p12 chr20: 18,195,309-18,510,763 ZNF133, SEC23B, 17 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4634280copy number variation1nstd183human GRCh37 chr20: 18,208,790-19,102,422 , GRCh38.p12 chr20: 18,228,146-19,121,778 , RNA5SP476, 30 more genes
    nsv4624254copy number variation1nstd183human GRCh37 chr20: 18,468,225-18,469,193 , GRCh38.p12 chr20: 18,487,581-18,488,549 RBBP9
    nsv4515295mobile element insertion1nstd166human GRCh37.p13 chr20: 18,472,256-18,472,256 , GRCh38.p12 chr20: 18,491,612-18,491,612 RBBP9
    nsv4457833copy number variation1nstd102humanUncertain significance GRCh37 chr20: 18,326,965-18,735,636 , GRCh38.p12 chr20: 18,346,321-18,754,992 DTD1-AS1, RNU6ATAC34P, 16 more genes
    nsv4350090copy number variation1nstd102humanPathogenic GRCh37 chr20: 11,716,825-19,331,055 , GRCh38.p12 chr20: 11,736,177-19,350,411 ENSAP1, BANF2, 107 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
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv4278536copy number variation1nstd166human GRCh37.p13 chr20: 18,477,250-18,478,644 , GRCh38.p12 chr20: 18,496,606-18,498,000 RBBP9
    nsv3966229copy number variation1nstd168human GRCh38 chr20: 18,466,890-18,492,893 , GRCh37.p13 chr20: 18,447,534-18,473,537 RPL21P3, MIR3192, 3 more genes
    nsv3927207copy number variation1nstd167human GRCh37 chr20: 18,466,779-18,466,816 , GRCh38.p12 chr20: 18,486,135-18,486,172 RBBP9, RPL21P3
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