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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906550copy number variation1nstd209human GRCh38 chr2: 200,971,755-200,972,632 , GRCh37.p13 chr2: 201,836,478-201,837,355 HYCC2, LOC105373835
    nsv5904102copy number variation1nstd209human GRCh38 chr2: 200,981,868-200,988,257 , GRCh37.p13 chr2: 201,846,591-201,852,980 HYCC2, LOC105373835
    nsv5897434copy number variation1nstd209human GRCh38 chr2: 201,013,442-201,013,504 , GRCh37.p13 chr2: 201,878,165-201,878,227 HYCC2, LOC105373835
    nsv5892797copy number variation1nstd209human GRCh38 chr2: 201,024,494-201,024,547 , GRCh37.p13 chr2: 201,889,217-201,889,270 HYCC2
    nsv5832362copy number variation1nstd209human GRCh38 chr2: 201,028,793-201,032,775 , GRCh37.p13 chr2: 201,893,516-201,897,498 HYCC2
    nsv5831845copy number variation1nstd209human GRCh38 chr2: 201,029,530-201,030,800 , GRCh37.p13 chr2: 201,894,253-201,895,523 HYCC2
    nsv5724074mobile element insertion1nstd211human GRCh38 chr2: 201,014,416-201,014,416 , GRCh37.p13 chr2: 201,879,139-201,879,139 HYCC2, LOC105373835
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452613copy number variation1nstd206human GRCh38 chr2: 201,024,494-201,024,550 , GRCh37.p13 chr2: 201,889,217-201,889,273 HYCC2
    nsv5449575copy number variation1nstd206human GRCh38 chr2: 200,971,757-200,972,633 , GRCh37.p13 chr2: 201,836,480-201,837,356 HYCC2, LOC105373835
    nsv5449374copy number variation1nstd206human GRCh38 chr2: 201,036,734-201,043,000 , GRCh37.p13 chr2: 201,901,457-201,907,723 HYCC2
    nsv5447424copy number variation1nstd206human GRCh38 chr2: 201,013,444-201,013,505 , GRCh37.p13 chr2: 201,878,167-201,878,228 HYCC2, LOC105373835
    nsv5445972copy number variation1nstd206human GRCh38 chr2: 201,048,489-201,050,249 , GRCh37.p13 chr2: 201,913,212-201,914,972 HYCC2
    nsv5445928copy number variation1nstd206human GRCh38 chr2: 201,056,003-201,062,524 , GRCh37.p13 chr2: 201,920,726-201,927,247 HYCC2, HNRNPA1P35
    nsv5442211copy number variation1nstd206human GRCh38 chr2: 201,020,375-201,020,426 , GRCh37.p13 chr2: 201,885,098-201,885,149 HYCC2
    nsv5361173translocation1nstd200human GRCh38 chr2: 201,031,442-201,031,442 , GRCh38 chr2: 201,031,153-201,031,153 , GRCh37.p13 chr2: 201,896,165-201,896,165 , GRCh37.p13 chr2: 201,895,876-201,895,876 HYCC2
    nsv5361172translocation1nstd200human GRCh38 chr2: 201,013,505-201,013,505 , GRCh38 chr2: 201,013,444-201,013,444 , GRCh37.p13 chr2: 201,878,167-201,878,167 , GRCh37.p13 chr2: 201,878,228-201,878,228 LOC105373835, HYCC2
    nsv5361171translocation1nstd200human GRCh38 chr2: 200,981,873-200,981,873 , GRCh38 chr2: 200,988,258-200,988,258 , GRCh37.p13 chr2: 201,846,596-201,846,596 , GRCh37.p13 chr2: 201,852,981-201,852,981 HYCC2, LOC105373835
    nsv5361170translocation1nstd200human GRCh38 chr2: 200,972,633-200,972,633 , GRCh38 chr2: 200,971,757-200,971,757 , GRCh37.p13 chr2: 201,836,480-201,836,480 , GRCh37.p13 chr2: 201,837,356-201,837,356 LOC105373835, HYCC2
    nsv5339768translocation1nstd200human GRCh37 chr2: 201,846,596-201,846,596 , GRCh37 chr2: 201,852,981-201,852,981 , GRCh38.p12 chr2: 200,988,258-200,988,258 , GRCh38.p12 chr2: 200,981,873-200,981,873 HYCC2, LOC105373835
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