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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976399inversion1nstd209human GRCh38 chr22: 17,577,704-20,098,016 , GRCh37.p13 chr22: 18,057,770-20,703,815 , ARVCF, 90 more genes
    nsv5951638copy number variation1nstd209human GRCh38 chr22: 17,735,737-17,736,564 , GRCh37.p13 chr22: 18,218,503-18,219,330 BID
    nsv5950291copy number variation1nstd209human GRCh38 chr22: 17,763,312-17,763,899 , GRCh37.p13 chr22: 18,246,078-18,246,665 BID, MIR3198-1
    nsv5665831insertion1nstd207human GRCh38 chr22: 17,753,958-17,753,958 , GRCh37.p13 chr22: 18,236,724-18,236,724 BID
    nsv5585553copy number variation1nstd207human GRCh38 chr22: 17,756,432-17,756,484 , GRCh37.p13 chr22: 18,239,198-18,239,250 BID
    nsv5550683copy number variation1nstd206human GRCh38 chr22: 17,750,560-17,751,151 , GRCh37.p13 chr22: 18,233,326-18,233,917 BID
    nsv5549228copy number variation1nstd206human GRCh38 chr22: 17,735,766-17,736,565 , GRCh37.p13 chr22: 18,218,532-18,219,331 BID
    nsv5540372copy number variation1nstd206human GRCh38 chr22: 17,739,575-17,739,728 , GRCh37.p13 chr22: 18,222,341-18,222,494 BID
    nsv5537960copy number variation1nstd206human GRCh38 chr22: 17,743,258-17,743,323 , GRCh37.p13 chr22: 18,226,024-18,226,089 BID
    nsv5375600translocation1nstd200human GRCh38 chr22: 17,770,876-17,770,876 , GRCh38 chr22: 17,771,809-17,771,809 , GRCh37.p13 chr22: 18,254,575-18,254,575 , GRCh37.p13 chr22: 18,253,642-18,253,642 BID
    nsv5375599translocation1nstd200human GRCh38 chr22: 17,770,872-17,770,872 , GRCh38 chr22: 17,772,144-17,772,144 , GRCh37.p13 chr22: 18,253,638-18,253,638 , GRCh37.p13 chr22: 18,254,910-18,254,910 BID
    nsv5375598translocation1nstd200human GRCh38 chr22: 17,768,699-17,768,699 , GRCh38 chr22: 17,764,618-17,764,618 , GRCh37.p13 chr22: 18,247,384-18,247,384 , GRCh37.p13 chr22: 18,251,465-18,251,465 BID, MIR3198-1
    nsv5360387translocation1nstd200human GRCh38 chr22: 17,735,766-17,735,766 , GRCh38 chr22: 17,736,565-17,736,565 , GRCh37.p13 chr22: 18,218,532-18,218,532 , GRCh37.p13 chr22: 18,219,331-18,219,331 BID
    nsv5324120copy number variation1nstd204human GRCh38.p13 chr22: 17,757,582-17,759,121 , GRCh37.p13 chr22: 18,240,348-18,241,887 BID
    nsv5287395copy number variation1nstd204human GRCh38.p13 chr22: 17,757,536-17,759,055 , GRCh37.p13 chr22: 18,240,302-18,241,821 BID
    nsv4868971copy number variation1nstd200human GRCh37 chr22: 18,240,356-18,241,872 , GRCh38.p12 chr22: 17,757,590-17,759,106 BID
    nsv4868970copy number variation1nstd200human GRCh37 chr22: 18,218,532-18,219,331 , GRCh38.p12 chr22: 17,735,766-17,736,565 BID
    nsv4769389copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,800,000-21,500,000 , GRCh38.p12 chr22: 16,367,190-21,145,711 POM121L15P, TRMT2A, 192 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4760760insertion1nstd199human GRCh37 chr22: 18,236,778-18,236,778 , GRCh38.p12 chr22: 17,754,012-17,754,012 BID
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