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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097528copy number variation1nstd102humanPathogenic GRCh37 chr5: 178,408,658-178,772,329 , GRCh38.p12 chr5: 178,981,657-179,345,328 GRM6, ADAMTS2, 4 more genes
    nsv7097527copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,408,658-178,585,900 , GRCh38.p12 chr5: 178,981,657-179,158,899 ADAMTS2, ZNF354C, 3 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7096770copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,413,111-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 1-602,153 , GRCh38.p12 chr5: 178,986,110-179,836,593 HMGB3P22, MAML1, 25 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7039490inversion1nstd229human GRCh38 chr5: 178,862,687-179,212,396 , GRCh37.p13 chr5: 178,289,688-178,639,397 ZNF354C, ZNF454, 10 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv7038226inversion1nstd229human GRCh38 chr5: 178,840,029-179,299,240 , GRCh37.p13 chr5: 178,267,030-178,726,241 ZFP2, LOC100288803, 11 more genes
    nsv6795790copy number variation1nstd229human GRCh38 chr5: 178,442,220-179,237,764 , GRCh37.p13 chr5: 177,869,221-178,664,765 LOC100288803, RN7SKP70, 18 more genes
    nsv6789520copy number variation1nstd229human GRCh38 chr5: 179,055,124-179,058,675 , GRCh37.p13 chr5: 178,482,125-178,485,676 ZNF354C
    nsv6789361copy number variation1nstd229human GRCh38 chr5: 178,862,701-179,244,300 , GRCh37.p13 chr5: 178,289,702-178,671,301 RNU1-39P, GRM6, 10 more genes
    nsv6787632copy number variation1nstd229human GRCh38 chr5: 178,858,379-179,340,876 , GRCh37.p13 chr5: 178,285,380-178,767,877 ZNF354B, LOC100422593, 10 more genes
    nsv6783936copy number variation1nstd229human GRCh38 chr5: 179,001,210-179,275,953 , GRCh37.p13 chr5: 178,428,211-178,702,954 ZNF879, ADAMTS2, 1 more genes
    nsv6781251copy number variation1nstd229human GRCh38 chr5: 178,256,072-179,080,937 , GRCh37.p13 chr5: 177,683,073-178,507,938 ZNF354B, ZNF354A, 20 more genes
    nsv6636731copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,125,235-178,759,093 , GRCh38.p12 chr5: 178,698,234-179,332,092 LOC100422593, ZNF879, 14 more genes
    nsv6636440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,746,012-179,975,280 , GRCh38.p12 chr5: 178,319,011-180,548,280 RUFY1-AS1, RPS15AP18, 60 more genes
    nsv6636428copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,507,587-178,922,733 , GRCh38.p12 chr5|NW_016107298.1: 1-260,378 , GRCh38.p12 chr5: 179,080,586-179,495,732 LOC105377759, ADAMTS2, 2 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630568copy number variation1nstd224human GRCh37 chr5: 178,165,521-178,936,722 , GRCh38.p12 chr5: 178,738,520-179,509,721 ADAMTS2, ZNF354C, 15 more genes
    nsv6630511copy number variation1nstd224human GRCh37 chr5: 178,400,860-178,983,987 , GRCh38.p12 chr5: 178,973,859-179,556,986 , GRCh38.p12 chr5|NW_016107298.1: 1-321,626 GRM6, ZNF354C, 9 more genes
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