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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5465523copy number variation1nstd206human GRCh38 chr5: 177,669,324-179,310,000 , GRCh37.p13 chr5: 177,096,325-178,737,001 , LOC100129457, 48 more genes
    nsv5228269copy number variation1nstd204human GRCh38.p13 chr5: 179,075,639-179,099,087 , GRCh37.p13 chr5: 178,502,640-178,526,088 ZNF354C
    nsv4940114copy number variation1nstd200human GRCh38 chr5: 178,985,568-179,789,759 , GRCh37.p13 chr5: 178,412,569-179,216,760 , LOC100884169, 21 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4729181copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,397,713-178,730,385 , GRCh38.p12 chr5: 178,970,712-179,303,384 ADAMTS2, ZNF354C, 3 more genes
    nsv4675130copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,487,249-180,622,216 , GRCh38.p12 chr5: 179,060,248-181,195,216 OR2V2, TRV-AAC1-2, 81 more genes
    nsv4597957copy number variation1nstd183human GRCh37 chr5: 178,415,937-178,866,013 , GRCh38.p12 chr5: 178,988,936-179,439,012 GRM6, ADAMTS2, 5 more genes
    nsv4592948copy number variation2nstd183human GRCh37 chr5: 178,507,267-178,510,456 , GRCh38.p12 chr5: 179,080,266-179,083,455 ZNF354C
    nsv4590810copy number variation1nstd183human GRCh37 chr5: 178,507,261-178,514,088 , GRCh38.p12 chr5: 179,080,260-179,087,087 ZNF354C
    nsv4457212copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,643,613-179,085,551 , GRCh38.p12 chr5: 177,216,612-179,658,550 LOC100502572, PIGFP1, 79 more genes
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
    nsv4455282copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,788,681-178,982,549 , GRCh38.p12 chr5: 178,361,680-179,555,548 PIGFP1, COL23A1, 26 more genes
    nsv4406781copy number variation1nstd174human GRCh37 chr5: 178,423,101-178,866,001 , GRCh38.p12 chr5: 178,996,100-179,439,000 ADAMTS2, ZNF354C, 4 more genes
    nsv4350559copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,990,352-180,690,937 , GRCh38.p12 chr5: 175,563,349-181,263,936 FAF2, ARL10, 198 more genes
    nsv4350315copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 177,776,148-180,687,012 , GRCh38.p12 chr5: 178,349,147-181,260,011 CANX, FOXO1B, 114 more genes
    nsv4347913copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 175,843,728-180,703,728 , GRCh38.p12 chr5: 176,416,727-181,276,727 CANX, CLTB, 177 more genes
    nsv4119351copy number variation1nstd166human GRCh37.p13 chr5: 178,482,124-178,485,675 , GRCh38.p12 chr5: 179,055,123-179,058,674 ZNF354C
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3922812copy number variation1nstd102humanPathogenic NCBI36 chr5: 176,059,735-180,629,412 , GRCh38 chr5: 176,700,128-181,269,805 , GRCh37 chr5: 176,127,129-180,696,806 MRPL50P3, SUDS3P1, 167 more genes
    nsv3922225copy number variation1nstd102humanLikely benign GRCh37 chr5: 178,415,365-179,020,558 , NCBI36 chr5: 178,347,971-178,953,164 , GRCh38 chr5: 178,988,364-179,593,557 LOC105377762, LOC100288803, 10 more genes
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