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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5470145copy number variation1nstd206human GRCh38 chr5: 142,429,551-143,065,626 , GRCh37.p13 chr5: 141,809,116-142,445,191 FGF1, ARHGAP26, 5 more genes
    nsv5310412copy number variation1nstd204human GRCh38.p13 chr5: 142,485,295-142,836,020 , GRCh37.p13 chr5: 141,864,860-142,215,585 FGF1, RPS12P10, 2 more genes
    nsv5235065copy number variation1nstd204human GRCh38.p13 chr5: 142,485,201-142,836,000 , GRCh37.p13 chr5: 141,864,766-142,215,565 ARHGAP26, FGF1, 2 more genes
    nsv5087881mobile element insertion1nstd203human GRCh38 chr5: 142,752,909-142,752,923 , GRCh37.p13 chr5: 142,132,474-142,132,488 LINC01844
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945174copy number variation1nstd200human GRCh38 chr5: 142,682,367-143,391,234 , GRCh37.p13 chr5: 142,061,932-142,770,799 NR3C1, RPL7P21, 6 more genes
    nsv4938989copy number variation1nstd200human GRCh38 chr5: 142,754,028-142,755,343 , GRCh37.p13 chr5: 142,133,593-142,134,908 LINC01844
    nsv4938988copy number variation1nstd200human GRCh38 chr5: 142,749,111-142,753,540 , GRCh37.p13 chr5: 142,128,676-142,133,105 LINC01844
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805882copy number variation1nstd200human GRCh37 chr5: 142,061,932-142,770,799 , GRCh38.p12 chr5: 142,682,367-143,391,234 ARHGAP26-AS1, FGF1, 6 more genes
    nsv4804265copy number variation1nstd200human GRCh37 chr5: 142,133,593-142,134,908 , GRCh38.p12 chr5: 142,754,028-142,755,343 LINC01844
    nsv4680271copy number variation1nstd189human GRCh37.p13 chr5: 141,886,549-142,264,406 , GRCh38.p12 chr5: 142,506,984-142,884,841 FGF1, ARHGAP26, 3 more genes
    nsv4597787copy number variation1nstd183human GRCh37 chr5: 141,893,763-142,399,583 , GRCh38.p12 chr5: 142,514,198-143,020,018 FGF1, ARHGAP26, 4 more genes
    nsv4590197copy number variation1nstd183human GRCh37 chr5: 141,882,819-142,249,382 , GRCh38.p12 chr5: 142,503,254-142,869,817 ARHGAP26, ARHGAP26-AS1, 3 more genes
    nsv4522944copy number variation1nstd166human GRCh37.p13 chr5: 142,088,999-142,129,000 , GRCh38.p12 chr5: 142,709,434-142,749,435 LINC01844
    nsv4457090copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436 PCDHGC4, CKS1BP5, 165 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4412222copy number variation1nstd174human GRCh37 chr5: 141,809,116-142,445,189 , GRCh38.p12 chr5: 142,429,551-143,065,624 FGF1, ARHGAP26, 5 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
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