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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967739inversion1nstd209human GRCh38 chr10: 27,341,069-27,367,322 , GRCh37.p13 chr10: 27,629,998-27,656,251 FAM210CP, LINC02673
    nsv5921613copy number variation1nstd209human GRCh38 chr10: 27,314,818-27,417,440 , GRCh37.p13 chr10: 27,603,747-27,706,369 PTCHD3, FAM210CP, 5 more genes
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5910368copy number variation1nstd209human GRCh38 chr10: 27,348,162-27,348,222 , GRCh37.p13 chr10: 27,637,091-27,637,151 FAM210CP
    nsv5907621copy number variation1nstd209human GRCh38 chr10: 27,349,325-27,353,166 , GRCh37.p13 chr10: 27,638,254-27,642,095 FAM210CP
    nsv5854781copy number variation1nstd209human GRCh38 chr10: 27,349,294-27,353,186 , GRCh37.p13 chr10: 27,638,223-27,642,115 FAM210CP
    nsv5853323copy number variation1nstd209human GRCh38 chr10: 27,339,663-27,349,293 , GRCh37.p13 chr10: 27,628,592-27,638,222 FAM210CP, LINC02673
    nsv5590200copy number variation1nstd207human GRCh38 chr10: 27,349,327-27,353,166 , GRCh37.p13 chr10: 27,638,256-27,642,095 FAM210CP
    nsv5587869copy number variation1nstd207human GRCh38 chr10: 27,348,162-27,348,222 , GRCh37.p13 chr10: 27,637,091-27,637,151 FAM210CP
    nsv5492877copy number variation1nstd206human GRCh38 chr10: 27,314,819-27,417,441 , GRCh37.p13 chr10: 27,603,748-27,706,370 PTCHD3, FAM210CP, 5 more genes
    nsv5483050copy number variation1nstd206human GRCh38 chr10: 27,042,537-27,369,512 , GRCh37.p13 chr10: 27,331,466-27,658,441 RNU6-666P, ANKRD26, 12 more genes
    nsv5480838copy number variation1nstd206human GRCh38 chr10: 27,349,325-27,353,167 , GRCh37.p13 chr10: 27,638,254-27,642,096 FAM210CP
    nsv5473925copy number variation1nstd206human GRCh38 chr10: 27,138,085-27,696,804 , GRCh37.p13 chr10: 27,427,014-27,985,733 TRIAP1P1, RNU2-24P, 15 more genes
    nsv5315732copy number variation1nstd204human GRCh38.p13 chr10: 27,314,797-27,417,461 , GRCh37.p13 chr10: 27,603,726-27,706,390 PTCHD3, FAM210CP, 5 more genes
    nsv5304787copy number variation1nstd204human GRCh38.p13 chr10: 27,349,325-27,353,167 , GRCh37.p13 chr10: 27,638,254-27,642,096 FAM210CP
    nsv5256754copy number variation1nstd204human GRCh38.p13 chr10: 27,349,301-27,355,900 , GRCh37.p13 chr10: 27,638,230-27,644,829 FAM210CP
    nsv5249682copy number variation1nstd204human GRCh38.p13 chr10: 27,349,301-27,350,400 , GRCh37.p13 chr10: 27,638,230-27,639,329 FAM210CP
    nsv5244567copy number variation1nstd204human GRCh38.p13 chr10: 27,345,601-27,355,200 , GRCh37.p13 chr10: 27,634,530-27,644,129 FAM210CP
    nsv5243569copy number variation1nstd204human GRCh38.p13 chr10: 27,350,601-27,353,200 , GRCh37.p13 chr10: 27,639,530-27,642,129 FAM210CP
    nsv5243215copy number variation1nstd204human GRCh38.p13 chr10: 27,341,401-27,353,100 , GRCh37.p13 chr10: 27,630,330-27,642,029 LINC02673, FAM210CP
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