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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6796438copy number variation1nstd229human GRCh38 chr6: 46,726,621-46,727,021 , GRCh37.p13 chr6: 46,694,358-46,694,758 PLA2G7
    nsv6791491copy number variation1nstd229human GRCh38 chr6: 46,686,072-46,936,489 , GRCh37.p13 chr6: 46,653,809-46,904,226 LOC105375080, ANKRD66, 6 more genes
    nsv6787281copy number variation1nstd229human GRCh38 chr6: 46,708,975-46,723,712 , GRCh37.p13 chr6: 46,676,712-46,691,449 PLA2G7
    nsv6779163copy number variation1nstd229human GRCh38 chr6: 46,702,773-46,703,130 , GRCh37.p13 chr6: 46,670,510-46,670,867 PLA2G7, TDRD6
    nsv6779127copy number variation1nstd229human GRCh38 chr6: 46,715,834-46,716,725 , GRCh37.p13 chr6: 46,683,571-46,684,462 PLA2G7
    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
    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
    nsv6169857copy number variation1nstd214human GRCh38 chr6: 46,712,500-46,712,576 , GRCh37.p13 chr6: 46,680,237-46,680,313 PLA2G7
    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
    nsv6003117copy number variation1nstd212human GRCh38 chr6: 46,734,415-46,734,476 , GRCh37.p13 chr6: 46,702,152-46,702,213 PLA2G7
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5228191copy number variation1nstd204human GRCh38.p13 chr6: 46,713,527-46,714,726 , GRCh37.p13 chr6: 46,681,264-46,682,463 PLA2G7
    nsv4816286copy number variation1nstd200human GRCh37 chr6: 46,680,946-46,682,704 , GRCh38.p12 chr6: 46,713,209-46,714,967 PLA2G7
    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
    nsv4749658copy number variation1nstd199human GRCh37 chr6: 46,702,161-46,702,221 , GRCh38.p12 chr6: 46,734,424-46,734,484 PLA2G7
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4593621copy number variation1nstd183human GRCh37 chr6: 46,625,635-46,669,936 , GRCh38.p12 chr6: 46,657,898-46,702,199 TDRD6-AS1, SLC25A27, 2 more genes
    nsv4539680insertion1nstd166human GRCh37.p13 chr6: 46,689,225-46,689,225 , GRCh38.p12 chr6: 46,721,488-46,721,488 PLA2G7
    nsv4480711mobile element insertion1nstd166human GRCh37.p13 chr6: 46,676,398-46,676,398 , GRCh38.p12 chr6: 46,708,661-46,708,661 PLA2G7
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