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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907084copy number variation1nstd209human GRCh38 chr5: 179,629,443-179,629,497 , GRCh37.p13 chr5: 179,056,444-179,056,498 HNRNPH1
    nsv5892721copy number variation1nstd209human GRCh38 chr5: 179,524,543-179,651,938 , GRCh37.p13 chr5: 178,951,544-179,078,939 HNRNPH1, RUFY1, 6 more genes
    nsv5889182copy number variation1nstd209human GRCh38 chr5: 179,629,114-179,629,840 , GRCh37.p13 chr5: 179,056,115-179,056,841 HNRNPH1
    nsv5841941copy number variation1nstd209human GRCh38 chr5: 179,626,010-179,633,200 , GRCh37.p13 chr5: 179,053,011-179,060,201 HNRNPH1
    nsv5672210inversion1nstd207human GRCh37.p13 chr5: 179,060,844-179,085,555 , GRCh38 chr5: 179,633,843-179,658,554 HNRNPH1, C5orf60, 2 more genes
    nsv5643322insertion1nstd207human GRCh38 chr5: 179,629,735-179,629,735 , GRCh37.p13 chr5: 179,056,736-179,056,736 HNRNPH1
    nsv5625020insertion1nstd207human GRCh38 chr5: 179,629,156-179,629,156 , GRCh37.p13 chr5: 179,056,157-179,056,157 HNRNPH1
    nsv5584050copy number variation1nstd207human GRCh38 chr5: 179,629,443-179,629,497 , GRCh37.p13 chr5: 179,056,444-179,056,498 HNRNPH1
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5472936copy number variation1nstd206human GRCh38 chr5: 179,629,003-179,630,567 , GRCh37.p13 chr5: 179,056,004-179,057,568 HNRNPH1
    nsv5472509copy number variation1nstd206human GRCh38 chr5: 179,629,151-179,632,162 , GRCh37.p13 chr5: 179,056,152-179,059,163 HNRNPH1
    nsv5468873copy number variation1nstd206human GRCh38 chr5: 179,616,019-179,616,111 , GRCh37.p13 chr5: 179,043,020-179,043,112 HNRNPH1
    nsv5459168copy number variation1nstd206human GRCh38 chr5: 179,629,114-179,629,860 , GRCh37.p13 chr5: 179,056,115-179,056,861 HNRNPH1
    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
    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
    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, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 more genes
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5300877copy number variation1nstd204human GRCh38.p13 chr5: 179,628,560-179,630,428 , GRCh37.p13 chr5: 179,055,561-179,057,429 HNRNPH1
    nsv5235860copy number variation1nstd204human GRCh38.p13 chr5: 179,633,801-179,638,100 , GRCh37.p13 chr5: 179,060,802-179,065,101 HNRNPH1
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