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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145031copy number variation1nstd232human GRCh37.p13 chr17: 45,475,411-45,475,459 , GRCh38.p12 chr17: 47,398,045-47,398,093 EFCAB13
    nsv7137094copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 44,949,883-46,507,482 , GRCh38.p12 chr17: 46,872,517-48,430,120 CDC27, ITGB3, 49 more genes
    nsv7073351inversion1nstd229human GRCh38 chr17: 47,363,306-47,363,377 , GRCh37.p13 chr17: 45,440,672-45,440,743 EFCAB13
    nsv6994805copy number variation1nstd229human GRCh38 chr17: 47,330,146-47,343,166 , GRCh37.p13 chr17: 45,407,512-45,420,532 EFCAB13
    nsv6993237copy number variation1nstd229human GRCh38 chr17: 47,404,679-47,406,926 , GRCh37.p13 chr17: 45,482,045-45,484,292 EFCAB13
    nsv6990806copy number variation1nstd229human GRCh38 chr17: 47,393,321-47,393,694 , GRCh37.p13 chr17: 45,470,687-45,471,060 EFCAB13
    nsv6989290copy number variation1nstd229human GRCh38 chr17: 47,346,466-47,351,327 , GRCh37.p13 chr17: 45,423,832-45,428,693 EFCAB13
    nsv6987322copy number variation1nstd229human GRCh38 chr17: 47,385,520-47,389,574 , GRCh37.p13 chr17: 45,462,886-45,466,940 EFCAB13
    nsv6985689copy number variation1nstd229human GRCh38 chr17: 47,356,518-47,357,922 , GRCh37.p13 chr17: 45,433,884-45,435,288 EFCAB13
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6980823copy number variation1nstd229human GRCh38 chr17: 47,408,468-47,443,918 , GRCh37.p13 chr17: 45,485,834-45,521,284 EFCAB13, NFE2L3P2
    nsv6980724copy number variation1nstd229human GRCh38 chr17: 47,348,965-47,349,373 , GRCh37.p13 chr17: 45,426,331-45,426,739 EFCAB13
    nsv6979496copy number variation1nstd229human GRCh38 chr17: 47,422,718-47,440,575 , GRCh37.p13 chr17: 45,500,084-45,517,941 EFCAB13, NFE2L3P2
    nsv6624250copy number variation2nstd224human GRCh37 chr17: 45,479,497-45,492,254 , GRCh38.p12 chr17: 47,402,131-47,414,888 EFCAB13
    nsv6624249copy number variation1nstd224human GRCh37 chr17: 45,447,802-45,468,871 , GRCh38.p12 chr17: 47,370,436-47,391,505 EFCAB13
    nsv6624248copy number variation1nstd224human GRCh37 chr17: 45,419,305-45,438,876 , GRCh38.p12 chr17: 47,341,939-47,361,510 EFCAB13
    nsv6624090copy number variation1nstd224human GRCh37 chr17: 45,479,497-45,504,870 , GRCh38.p12 chr17: 47,402,131-47,427,504 EFCAB13, NFE2L3P2
    nsv6624089copy number variation1nstd224human GRCh37 chr17: 45,435,575-45,451,990 , GRCh38.p12 chr17: 47,358,209-47,374,624 LOC100421523, EFCAB13
    nsv6624088copy number variation1nstd224human GRCh37 chr17: 45,435,575-45,447,832 , GRCh38.p12 chr17: 47,358,209-47,370,466 LOC100421523, EFCAB13
    nsv6624087copy number variation2nstd224human GRCh37 chr17: 45,419,305-45,468,871 , GRCh38.p12 chr17: 47,341,939-47,391,505 LOC100421523, EFCAB13
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