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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6797067copy number variation1nstd229human GRCh38 chr6: 46,598,901-46,675,200 , GRCh37.p13 chr6: 46,566,638-46,642,937 TDRD6-AS1, SLC25A27, 1 more genes
    nsv6793378copy number variation1nstd229human GRCh38 chr6: 46,651,967-46,652,668 , GRCh37.p13 chr6: 46,619,704-46,620,405 SLC25A27, CYP39A1
    nsv6790279copy number variation1nstd229human GRCh38 chr6: 46,663,201-46,665,800 , GRCh37.p13 chr6: 46,630,938-46,633,537 SLC25A27
    nsv6781574copy number variation1nstd229human GRCh38 chr6: 46,676,875-46,677,224 , GRCh37.p13 chr6: 46,644,612-46,644,961 SLC25A27, TDRD6-AS1
    nsv6778346copy number variation1nstd229human GRCh38 chr6: 46,657,985-46,674,730 , GRCh37.p13 chr6: 46,625,722-46,642,467 TDRD6-AS1, SLC25A27
    nsv6631063copy number variation1nstd224human GRCh37 chr6: 46,570,856-46,705,994 , GRCh38.p12 chr6: 46,603,119-46,738,257 TDRD6-AS1, PLA2G7, 3 more genes
    nsv6573924inversion1nstd223human GRCh38 chr6: 46,656,532-46,657,162 , GRCh37.p13 chr6: 46,624,269-46,624,899 SLC25A27
    nsv6570411inversion1nstd223human GRCh38 chr6: 46,656,397-46,657,148 , GRCh37.p13 chr6: 46,624,134-46,624,885 SLC25A27
    nsv6414397copy number variation1nstd223human GRCh38 chr6: 46,645,801-46,661,500 , GRCh37.p13 chr6: 46,613,538-46,629,237 SLC25A27, CYP39A1
    nsv6414229copy number variation1nstd223human GRCh38 chr6: 46,650,201-46,657,500 , GRCh37.p13 chr6: 46,617,938-46,625,237 SLC25A27, CYP39A1
    nsv6404657copy number variation1nstd223human GRCh38 chr6: 46,674,003-46,674,443 , GRCh37.p13 chr6: 46,641,740-46,642,180 SLC25A27, TDRD6-AS1
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5305233copy number variation1nstd204human GRCh37.p13 chr6: 46,644,913-46,645,807 , GRCh38.p13 chr6: 46,677,176-46,678,070 TDRD6-AS1, SLC25A27
    nsv5100430mobile element insertion1nstd203human GRCh38 chr6: 46,658,404-46,658,419 , GRCh37.p13 chr6: 46,626,141-46,626,156 SLC25A27
    nsv4934701copy number variation1nstd200human GRCh38 chr6: 46,674,687-46,689,020 , GRCh37.p13 chr6: 46,642,424-46,656,757 TDRD6-AS1, SLC25A27, 1 more genes
    nsv4828683copy number variation1nstd200human GRCh37 chr6: 46,642,424-46,656,757 , GRCh38.p12 chr6: 46,674,687-46,689,020 SLC25A27, TDRD6, 1 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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