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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5882400copy number variation1nstd209human GRCh38 chr2: 101,297,211-101,297,268 , GRCh37.p13 chr2: 101,913,673-101,913,730 RNF149
    nsv5872084copy number variation1nstd209human GRCh38 chr2: 101,295,088-101,295,884 , GRCh37.p13 chr2: 101,911,550-101,912,346 RNF149
    nsv5692492mobile element insertion1nstd211human GRCh38 chr2: 101,294,107-101,294,107 , GRCh37.p13 chr2: 101,910,569-101,910,569 RNF149
    nsv5690675mobile element insertion1nstd211human GRCh38 chr2: 101,292,431-101,292,431 , GRCh37.p13 chr2: 101,908,893-101,908,893 RNF149
    nsv5676429mobile element insertion1nstd211human GRCh38 chr2: 101,294,230-101,294,230 , GRCh37.p13 chr2: 101,910,692-101,910,692 RNF149
    nsv5578500copy number variation1nstd207human GRCh38 chr2: 101,297,211-101,297,268 , GRCh37.p13 chr2: 101,913,673-101,913,730 RNF149
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5445418copy number variation1nstd206human GRCh38 chr2: 101,297,217-101,297,269 , GRCh37.p13 chr2: 101,913,679-101,913,731 RNF149
    nsv5440089copy number variation1nstd206human GRCh38 chr2: 101,296,979-101,299,029 , GRCh37.p13 chr2: 101,913,441-101,915,491 RNF149
    nsv5406198mobile element insertion1nstd206human GRCh38 chr2: 101,292,431-101,292,482 , GRCh37.p13 chr2: 101,908,893-101,908,944 RNF149
    nsv5399560mobile element insertion1nstd206human GRCh38 chr2: 101,294,230-101,294,281 , GRCh37.p13 chr2: 101,910,692-101,910,743 RNF149
    nsv5281322copy number variation1nstd204human GRCh38.p13 chr2: 100,864,060-101,514,976 , GRCh37.p13 chr2: 101,480,522-102,131,438 LINC01870, LOC105373511, 17 more genes
    nsv5217676copy number variation1nstd204human GRCh38.p13 chr2: 100,959,101-101,514,900 , GRCh37.p13 chr2: 101,575,563-102,131,362 RNF149, NPAS2, 17 more genes
    nsv5213131copy number variation1nstd204human GRCh38.p13 chr2: 101,225,986-101,280,641 , GRCh37.p13 chr2: 101,842,448-101,897,103 SNORD89, LOC105373511, 2 more genes
    nsv5204309copy number variation1nstd204human GRCh38.p13 chr2: 101,272,435-101,325,855 , GRCh37.p13 chr2: 101,888,897-101,942,317 RNF149, SNORD89, 2 more genes
    nsv5062017mobile element insertion1nstd203human GRCh38 chr2: 101,288,127-101,288,127 , GRCh37.p13 chr2: 101,904,589-101,904,589 RNF149
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894859copy number variation1nstd200human GRCh38 chr2: 101,275,592-101,277,759 , GRCh37.p13 chr2: 101,892,054-101,894,221 RNF149
    nsv4894856copy number variation1nstd200human GRCh38 chr2: 100,864,090-101,514,954 , GRCh37.p13 chr2: 101,480,552-102,131,416 CREG2, LOC105373510, 17 more genes
    nsv4892948copy number variation1nstd200human GRCh38 chr2: 101,301,307-101,301,411 , GRCh37.p13 chr2: 101,917,769-101,917,873 RNF149
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