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Items: 1 to 20 of 686

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952856insertion1nstd209human GRCh38 chr9: 6,639,668-6,639,668 , GRCh37.p13 chr9: 6,639,668-6,639,668 RPL23AP57, GLDC
    nsv5951667insertion1nstd209human GRCh38 chr9: 6,634,569-6,634,569 , GRCh37.p13 chr9: 6,634,569-6,634,569 GLDC
    nsv5948105insertion1nstd209human GRCh38 chr9: 6,590,233-6,590,233 , GRCh37.p13 chr9: 6,590,233-6,590,233 GLDC
    nsv5925070copy number variation1nstd209human GRCh38 chr9: 6,551,925-6,552,070 , GRCh37.p13 chr9: 6,551,925-6,552,070 GLDC
    nsv5925000copy number variation1nstd209human GRCh38 chr9: 6,632,944-6,632,995 , GRCh37.p13 chr9: 6,632,944-6,632,995 GLDC
    nsv5912079copy number variation1nstd209human GRCh38 chr9: 6,622,749-6,622,828 , GRCh37.p13 chr9: 6,622,749-6,622,828 GLDC
    nsv5907820copy number variation1nstd209human GRCh38 chr9: 6,637,887-6,637,967 , GRCh37.p13 chr9: 6,637,887-6,637,967 RPL23AP57, GLDC
    nsv5867038copy number variation1nstd209human GRCh38 chr9: 6,618,408-6,619,566 , GRCh37.p13 chr9: 6,618,408-6,619,566 GLDC
    nsv5865527copy number variation1nstd209human GRCh38 chr9: 6,552,811-6,554,044 , GRCh37.p13 chr9: 6,552,811-6,554,044 GLDC
    nsv5728425mobile element insertion2nstd211human GRCh38 chr9: 6,534,402-6,534,402 , GRCh37.p13 chr9: 6,534,402-6,534,402 GLDC
    nsv5722942mobile element insertion1nstd211human GRCh38 chr9: 6,560,903-6,560,903 , GRCh37.p13 chr9: 6,560,903-6,560,903 GLDC
    nsv5712476mobile element insertion1nstd211human GRCh38 chr9: 6,605,997-6,605,997 , GRCh37.p13 chr9: 6,605,997-6,605,997 GLDC
    nsv5711605mobile element insertion1nstd211human GRCh38 chr9: 6,534,386-6,534,386 , GRCh37.p13 chr9: 6,534,386-6,534,386 GLDC
    nsv5706244mobile element insertion1nstd211human GRCh38 chr9: 6,629,969-6,629,969 , GRCh37.p13 chr9: 6,629,969-6,629,969 GLDC
    nsv5704981mobile element insertion2nstd211human GRCh38 chr9: 6,590,233-6,590,233 , GRCh37.p13 chr9: 6,590,233-6,590,233 GLDC
    nsv5700304mobile element insertion2nstd211human GRCh38 chr9: 6,639,668-6,639,668 , GRCh37.p13 chr9: 6,639,668-6,639,668 RPL23AP57, GLDC
    nsv5696531mobile element insertion2nstd211human GRCh38 chr9: 6,585,514-6,585,514 , GRCh37.p13 chr9: 6,585,514-6,585,514 GLDC
    nsv5674174copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 6,602,089-6,604,804 , GRCh38.p12 chr9: 6,602,089-6,604,804 GLDC
    nsv5673967copy number variation1nstd102humanPathogenic GRCh37 chr9: 6,610,182-6,610,366 , GRCh38.p12 chr9: 6,610,182-6,610,366 GLDC
    nsv5673966copy number variation1nstd102humanPathogenic GRCh37 chr9: 6,602,089-6,620,339 , GRCh38.p12 chr9: 6,602,089-6,620,339 GLDC
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