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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096068copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,782,122-13,782,529 , GRCh38.p12 chr20: 13,801,476-13,801,883 NDUFAF5
    nsv7096067copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,775,474-13,775,597 , GRCh38.p12 chr20: 13,794,828-13,794,951 NDUFAF5
    nsv7096069copy number variation1nstd102humanUncertain significance GRCh37 chr20: 13,795,054-13,799,077 , GRCh38.p12 chr20: 13,814,408-13,818,431 NDUFAF5
    nsv7020597copy number variation1nstd229human GRCh38 chr20: 13,802,095-13,806,339 , GRCh37.p13 chr20: 13,782,741-13,786,985 NDUFAF5
    nsv5012664copy number variation1nstd200human GRCh38 chr20: 13,796,247-13,796,455 , GRCh37.p13 chr20: 13,776,893-13,777,101 NDUFAF5
    nsv4290471copy number variation1nstd166human GRCh37.p13 chr20: 13,794,924-13,801,721 , GRCh38.p12 chr20: 13,814,278-13,821,075 NDUFAF5
    nsv4535080copy number variation1nstd166human GRCh37.p13 chr20: 13,770,690-13,776,864 , GRCh38.p12 chr20: 13,790,044-13,796,218 NDUFAF5
    nsv4537309copy number variation1nstd166human GRCh37.p13 chr20: 13,773,353-13,776,864 , GRCh38.p12 chr20: 13,792,707-13,796,218 NDUFAF5
    nsv4535117copy number variation1nstd166human GRCh37.p13 chr20: 13,770,690-13,773,250 , GRCh38.p12 chr20: 13,790,044-13,792,604 NDUFAF5
    nsv4535140copy number variation1nstd166human GRCh37.p13 chr20: 13,787,743-13,787,973 , GRCh38.p12 chr20: 13,807,097-13,807,327 NDUFAF5
    nsv4278350copy number variation1nstd166human GRCh37.p13 chr20: 13,776,893-13,777,101 , GRCh38.p12 chr20: 13,796,247-13,796,455 NDUFAF5
    nsv3161811copy number variation1nstd151human GRCh37 chr20: 13,769,232-13,779,151 , GRCh38.p12 chr20: 13,788,586-13,798,505 NDUFAF5
    esv3226031copy number variation1estd209human GRCh37 chr20: 13,798,692-13,798,706 , GRCh38.p12 chr20: 13,818,046-13,818,060 NDUFAF5
    esv3226032copy number variation1estd209human GRCh37 chr20: 13,799,089-13,799,090 , GRCh38.p12 chr20: 13,818,443-13,818,444 NDUFAF5
    esv3226030copy number variation1estd209human GRCh37 chr20: 13,787,693-13,787,694 , GRCh38.p12 chr20: 13,807,047-13,807,048 NDUFAF5
    esv3226029copy number variation1estd209human GRCh37 chr20: 13,770,983-13,770,984 , GRCh38.p12 chr20: 13,790,337-13,790,338 NDUFAF5
    esv3226028copy number variation1estd209human GRCh37 chr20: 13,767,165-13,767,166 , GRCh38.p12 chr20: 13,786,519-13,786,520 NDUFAF5
    esv3556857copy number variation1estd215human GRCh37 chr20: 13,798,448-13,798,470 , GRCh38.p12 chr20: 13,817,802-13,817,824 NDUFAF5
    esv3391663copy number variation1estd59human NCBI36 chr20: 13,737,408-13,737,851 , GRCh37.p13 chr20: 13,789,408-13,789,851 , GRCh38.p12 chr20: 13,808,762-13,809,205 NDUFAF5
    esv3361748copy number variation1estd59human NCBI36 chr20: 13,748,019-13,748,300 , GRCh37.p13 chr20: 13,800,019-13,800,300 , GRCh38.p12 chr20: 13,819,373-13,819,654 NDUFAF5
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