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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098922copy number variation1nstd102humanUncertain significance GRCh38 chr20: 25,121,080-25,485,829 , GRCh37.p13 chr20: 25,101,716-25,466,465 LOC105372579, LOC100128078, 9 more genes
    nsv7096018copy number variation1nstd102humanUncertain significance GRCh37 chr20: 25,394,406-25,426,627 , GRCh38.p12 chr20: 25,413,770-25,445,991 GINS1
    nsv7095886copy number variation1nstd102humanUncertain significance GRCh37 chr20: 25,422,318-25,422,432 , GRCh38.p12 chr20: 25,441,682-25,441,796 GINS1
    nsv7095885copy number variation1nstd102humanUncertain significance GRCh37 chr20: 25,319,843-25,388,551 , GRCh38.p12 chr20: 25,339,207-25,407,915 GINS1, LOC105372581, 2 more genes
    nsv7095550copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,319,843-25,426,627 , GRCh38.p12 chr20: 25,339,207-25,445,991 LOC105372581, ABHD12, 2 more genes
    nsv7072915inversion1nstd229human GRCh38 chr20: 25,405,850-25,408,469 , GRCh37.p13 chr20: 25,386,486-25,389,105 LOC105372581, GINS1
    nsv7072071inversion1nstd229human GRCh38 chr20: 25,416,446-25,420,421 , GRCh37.p13 chr20: 25,397,082-25,401,057 GINS1
    nsv7037589copy number variation1nstd229human GRCh38 chr20: 25,433,518-25,434,175 , GRCh37.p13 chr20: 25,414,154-25,414,811 GINS1
    nsv7037094copy number variation1nstd229human GRCh38 chr20: 23,996,469-25,641,348 , GRCh37.p13 chr20: 23,977,106-25,621,984 CST7, LOC105372579, 28 more genes
    nsv7035867copy number variation1nstd229human GRCh38 chr20: 25,446,334-25,446,389 , GRCh37.p13 chr20: 25,426,970-25,427,025 GINS1
    nsv7035612copy number variation1nstd229human GRCh38 chr20: 25,387,087-25,463,713 , GRCh37.p13 chr20: 25,367,723-25,444,349 LOC105372581, ABHD12, 2 more genes
    nsv7035258copy number variation1nstd229human GRCh38 chr20: 24,250,776-25,542,572 , GRCh37.p13 chr20: 24,231,412-25,523,208 LOC105372581, LINC02967, 21 more genes
    nsv7035238copy number variation1nstd229human GRCh38 chr20: 25,186,524-25,487,024 , GRCh37.p13 chr20: 25,167,160-25,467,660 PPIAP2, PYGB, 7 more genes
    nsv7035203copy number variation1nstd229human GRCh38 chr20: 25,426,201-25,432,800 , GRCh37.p13 chr20: 25,406,837-25,413,436 GINS1
    nsv7035033copy number variation1nstd229human GRCh38 chr20: 25,297,347-25,497,977 , GRCh37.p13 chr20: 25,277,983-25,478,613 PYGB, ABHD12, 4 more genes
    nsv7033425copy number variation1nstd229human GRCh38 chr20: 25,447,443-25,467,604 , GRCh37.p13 chr20: 25,428,079-25,448,240 GINS1, NINL
    nsv7032096copy number variation1nstd229human GRCh38 chr20: 25,344,717-25,466,485 , GRCh37.p13 chr20: 25,325,353-25,447,121 NINL, PPIAP2, 3 more genes
    nsv7031716copy number variation1nstd229human GRCh38 chr20: 25,444,437-25,444,793 , GRCh37.p13 chr20: 25,425,073-25,425,429 GINS1
    nsv7030385copy number variation1nstd229human GRCh38 chr20: 25,429,901-25,433,100 , GRCh37.p13 chr20: 25,410,537-25,413,736 GINS1
    nsv7029572copy number variation1nstd229human GRCh38 chr20: 25,418,767-25,432,892 , GRCh37.p13 chr20: 25,399,403-25,413,528 GINS1
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