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Items: 1 to 20 of 184

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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
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7074650inversion1nstd229human GRCh38 chr20: 945,543-2,680,685 , GRCh37.p13 chr20: 926,186-2,661,331 , SDCBP2-AS1, 54 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7011542copy number variation1nstd229human GRCh38 chr20: 2,347,591-2,615,813 , GRCh37.p13 chr20: 2,328,237-2,596,459 TGM6, LOC105372505, 5 more genes
    nsv7011451copy number variation1nstd229human GRCh38 chr20: 2,048,209-2,717,834 , GRCh37.p13 chr20: 2,028,855-2,698,480 SNORD86, TGM3, 21 more genes
    nsv7004296copy number variation1nstd229human GRCh38 chr20: 2,534,501-2,538,700 , GRCh37.p13 chr20: 2,515,147-2,519,346 LOC105372504, TMC2
    nsv7001202copy number variation1nstd229human GRCh38 chr20: 2,534,345-2,534,443 , GRCh37.p13 chr20: 2,514,991-2,515,089 LOC105372504
    nsv6999024copy number variation1nstd229human GRCh38 chr20: 2,521,750-2,691,136 , GRCh37.p13 chr20: 2,502,396-2,671,782 NOP56, SNORD86, 12 more genes
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6532153copy number variation1nstd223human GRCh38 chr20: 2,534,329-2,534,443 , GRCh37.p13 chr20: 2,514,975-2,515,089 LOC105372504
    nsv6530639copy number variation1nstd223human GRCh38 chr20: 2,543,075-2,549,487 , GRCh37.p13 chr20: 2,523,721-2,530,133 TMC2, LOC105372504
    nsv6516474copy number variation1nstd223human GRCh38 chr20: 2,540,520-2,543,040 , GRCh37.p13 chr20: 2,521,166-2,523,686 TMC2, LOC105372504
    nsv6213393copy number variation1nstd214human GRCh38 chr20: 2,534,329-2,534,442 , GRCh37.p13 chr20: 2,514,975-2,515,088 LOC105372504
    nsv6124052copy number variation1nstd186human GRCh37 chr20: 2,514,991-2,515,089 , GRCh38.p12 chr20: 2,534,345-2,534,443 LOC105372504
    nsv6044500copy number variation1nstd212human GRCh38 chr20: 2,534,337-2,534,448 , GRCh37.p13 chr20: 2,514,983-2,515,094 LOC105372504
    nsv6041159copy number variation1nstd212human GRCh38 chr20: 2,542,709-2,543,921 , GRCh37.p13 chr20: 2,523,355-2,524,567 LOC105372504, TMC2
    nsv5938129copy number variation1nstd209human GRCh38 chr20: 2,530,778-2,535,154 , GRCh37.p13 chr20: 2,511,424-2,515,800 TMC2, LOC105372504
    nsv5932212copy number variation1nstd209human GRCh38 chr20: 2,534,329-2,534,442 , GRCh37.p13 chr20: 2,514,975-2,515,088 LOC105372504
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