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Items: 1 to 20 of 938

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145247copy number variation1nstd232human GRCh37.p13 chr5: 178,601,826-178,601,891 , GRCh38.p12 chr5: 179,174,825-179,174,890 ADAMTS2
    nsv7140151copy number variation1nstd232human GRCh37.p13 chr5: 178,641,141-178,641,290 , GRCh38.p12 chr5: 179,214,140-179,214,289 ADAMTS2
    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
    nsv7097137copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,748-178,772,329 , GRCh38.p12 chr5: 179,343,747-179,345,328 , GRCh38.p12 chr5|NW_016107298.1: 108,454-110,035 LOC105377759, ADAMTS2
    nsv7097136copy number variation1nstd102humanPathogenic GRCh37 chr5: 178,634,504-178,634,726 , GRCh38.p12 chr5: 179,207,503-179,207,725 ADAMTS2
    nsv7096771copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,540,868-178,700,085 , GRCh38.p12 chr5: 179,113,867-179,273,084 ADAMTS2
    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
    nsv7041034inversion1nstd229human GRCh38 chr5: 179,211,972-179,212,084 , GRCh37.p13 chr5: 178,638,973-178,639,085 ADAMTS2
    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
    nsv6797964copy number variation1nstd229human GRCh38 chr5: 179,247,413-179,259,976 , GRCh37.p13 chr5: 178,674,414-178,686,977 ADAMTS2
    nsv6797754copy number variation1nstd229human GRCh38 chr5: 179,333,515-179,341,452 , GRCh37.p13 chr5: 178,760,516-178,768,453 ADAMTS2
    nsv6796929copy number variation1nstd229human GRCh38 chr5: 179,217,701-179,224,100 , GRCh37.p13 chr5: 178,644,702-178,651,101 ADAMTS2
    nsv6796773copy number variation1nstd229human GRCh38 chr5: 179,132,701-179,193,200 , GRCh37.p13 chr5: 178,559,702-178,620,201 ADAMTS2
    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
    nsv6795305copy number variation1nstd229human GRCh38 chr5: 179,110,560-179,110,937 , GRCh37.p13 chr5: 178,537,561-178,537,938 ADAMTS2
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