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Items: 1 to 20 of 398

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978683insertion1nstd209human GRCh38 chr13: 49,730,519-49,730,519 , GRCh37.p13 chr13: 50,304,655-50,304,655 KPNA3
    nsv5940646copy number variation1nstd209human GRCh38 chr13: 49,755,684-49,756,834 , GRCh37.p13 chr13: 50,329,820-50,330,970 KPNA3
    nsv5935461copy number variation1nstd209human GRCh38 chr13: 49,706,926-49,708,171 , GRCh37.p13 chr13: 50,281,062-50,282,307 KPNA3
    nsv5724057mobile element insertion1nstd211human GRCh38 chr13: 49,789,521-49,789,521 , GRCh37.p13 chr13: 50,363,657-50,363,657 KPNA3
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5555663mobile element insertion1nstd206human GRCh38 chr13: 49,789,536-49,789,572 , GRCh37.p13 chr13: 50,363,672-50,363,708 KPNA3
    nsv5501460copy number variation1nstd206human GRCh38 chr13: 49,767,994-49,768,108 , GRCh37.p13 chr13: 50,342,130-50,342,244 KPNA3
    nsv5366539translocation1nstd200human GRCh38 chr2: 155,671,569-155,671,569 , GRCh38 chr13: 49,789,904-49,789,904 , GRCh37.p13 chr2: 156,528,081-156,528,081 , GRCh37.p13 chr13: 50,364,040-50,364,040 KPNA3
    nsv5307050copy number variation1nstd204human GRCh38.p13 chr13: 49,201,982-51,085,310 , GRCh37.p13 chr13: 49,776,118-51,659,446 , MLNR, 40 more genes
    nsv5187326mobile element insertion1nstd203human GRCh38 chr13: 49,789,521-49,789,521 , GRCh37.p13 chr13: 50,363,657-50,363,657 KPNA3
    nsv5180367mobile element insertion1nstd203human GRCh38 chr13: 49,775,992-49,776,006 , GRCh37.p13 chr13: 50,350,128-50,350,142 KPNA3
    nsv5158471mobile element insertion1nstd203human GRCh38 chr13: 49,704,710-49,704,724 , GRCh37.p13 chr13: 50,278,846-50,278,860 KPNA3
    nsv5155914mobile element insertion1nstd203human GRCh38 chr13: 49,730,519-49,730,555 , GRCh37.p13 chr13: 50,304,655-50,304,691 KPNA3
    nsv5152843mobile element insertion1nstd203human GRCh38 chr13: 49,767,577-49,767,593 , GRCh37.p13 chr13: 50,341,713-50,341,729 KPNA3
    nsv5144593mobile element insertion1nstd203human GRCh38 chr13: 49,790,905-49,790,918 , GRCh37.p13 chr13: 50,365,041-50,365,054 KPNA3
    nsv5004586copy number variation1nstd200human GRCh38 chr13: 49,779,759-49,780,253 , GRCh37.p13 chr13: 50,353,895-50,354,389 KPNA3
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4845274copy number variation1nstd200human GRCh37 chr13: 49,776,128-51,659,444 , GRCh38.p12 chr13: 49,201,992-51,085,308 , PHF11, 40 more genes
    nsv4837141copy number variation1nstd200human GRCh37 chr13: 50,353,899-50,354,389 , GRCh38.p12 chr13: 49,779,763-49,780,253 KPNA3
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