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Items: 1 to 20 of 2216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127923insertion1nstd186human GRCh37 chr5: 178,977,548-178,977,588 , GRCh38.p12 chr5: 179,550,547-179,550,587 , GRCh38.p12 chr5|NW_016107298.1: 315,081-315,229 LOC105377762, RUFY1
    nsv6127749insertion1nstd186human GRCh37 chr5: 179,122,509-179,122,528 , GRCh38.p12 chr5|NW_016107298.1: 461,065-461,084 , GRCh38.p12 chr5: 179,695,508-179,695,527 CANX
    nsv6119966copy number variation1nstd186human GRCh37 chr5: 178,838,673-178,839,438 , GRCh38.p12 chr5: 179,411,672-179,412,437 , GRCh38.p12 chr5|NW_016107298.1: 176,379-177,144 0
    nsv6119882copy number variation1nstd186human GRCh37 chr5: 178,935,608-178,937,767 , GRCh38.p12 chr5: 179,508,607-179,510,766 , GRCh38.p12 chr5|NW_016107298.1: 273,266-275,426 LOC100128622
    nsv6118390copy number variation1nstd186human GRCh37 chr5: 179,056,115-179,056,861 , GRCh38.p12 chr5|NW_016107298.1: 395,402-396,093 , GRCh38.p12 chr5: 179,629,114-179,629,860 HNRNPH1
    nsv6118020copy number variation1nstd186human GRCh37 chr5: 178,838,325-178,840,325 , GRCh38.p12 chr5: 179,411,324-179,413,324 , GRCh38.p12 chr5|NW_016107298.1: 176,031-178,031 0
    nsv6117922copy number variation1nstd186human GRCh37 chr5: 178,740,257-178,740,919 , GRCh38.p12 chr5: 179,313,256-179,313,918 , GRCh38.p12 chr5|NW_016107298.1: 77,963-78,625 ADAMTS2
    nsv5673584copy number variation1nstd102humanPathogenic GRCh37 chr5: 178,699,902-178,772,339 , GRCh38.p12 chr5: 179,272,901-179,345,338 , GRCh38.p12 chr5|NW_016107298.1: 37,608-110,045 LOC105377759, ADAMTS2
    nsv5389164copy number variation2nstd186human GRCh37 chr5: 179,056,109-179,056,894 , GRCh38.p12 chr5: 179,629,108-179,629,893 , GRCh38.p12 chr5|NW_016107298.1: 395,396-396,126 HNRNPH1
    nsv5388880copy number variation1nstd186human GRCh37 chr5: 178,691,866-178,692,061 , GRCh38.p12 chr5: 179,264,865-179,265,060 , GRCh38.p12 chr5|NW_016107298.1: 29,572-29,767 ADAMTS2
    nsv5388492copy number variation1nstd186human GRCh37 chr5: 178,740,303-178,740,527 , GRCh38.p12 chr5: 179,313,302-179,313,526 , GRCh38.p12 chr5|NW_016107298.1: 78,009-78,233 ADAMTS2
    nsv5388382copy number variation1nstd186human GRCh37 chr5: 178,856,545-178,856,913 , GRCh38.p12 chr5: 179,429,544-179,429,912 , GRCh38.p12 chr5|NW_016107298.1: 194,298-194,494 0
    nsv5388365copy number variation1nstd186human GRCh37 chr5: 178,801,418-178,801,622 , GRCh38.p12 chr5: 179,374,417-179,374,621 , GRCh38.p12 chr5|NW_016107298.1: 139,124-139,328 LOC107986494
    nsv5388265copy number variation1nstd186human GRCh37 chr5: 178,801,467-178,801,800 , GRCh38.p12 chr5: 179,374,466-179,374,799 , GRCh38.p12 chr5|NW_016107298.1: 139,173-139,506 LOC107986494
    nsv5388057copy number variation1nstd186human GRCh37 chr5: 178,936,148-178,937,325 , GRCh38.p12 chr5|NW_016107298.1: 273,805-274,982 , GRCh38.p12 chr5: 179,509,147-179,510,324 LOC100128622
    nsv5385895copy number variation1nstd186human GRCh37 chr5: 178,935,785-178,937,527 , GRCh38.p12 chr5: 179,508,784-179,510,526 , GRCh38.p12 chr5|NW_016107298.1: 273,443-275,184 LOC100128622
    nsv5385771copy number variation1nstd186human GRCh37 chr5: 179,056,136-179,057,178 , GRCh38.p12 chr5|NW_016107298.1: 395,423-396,410 , GRCh38.p12 chr5: 179,629,135-179,630,177 HNRNPH1
    nsv5381980mobile element deletion1nstd186human GRCh37 chr5: 178,672,486-178,672,804 , GRCh38.p12 chr5: 179,245,485-179,245,803 , GRCh38.p12 chr5|NW_016107298.1: 10,192-10,510 ADAMTS2
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 22 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 , GRCh38.p12 chr5: 179,343,757-179,836,603 LOC100502572, CBY3, 22 more genes
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