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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979328inversion1nstd209human GRCh38 chr19: 32,019,307-33,218,671 , GRCh37.p13 chr19: 32,510,213-33,709,577 , LRP3, 28 more genes
    nsv5932304copy number variation1nstd209human GRCh38 chr19: 32,361,660-32,361,792 , GRCh37.p13 chr19: 32,852,566-32,852,698 ZNF507
    nsv5708648mobile element insertion2nstd211human GRCh38 chr19: 32,350,626-32,350,626 , GRCh37.p13 chr19: 32,841,532-32,841,532 ZNF507
    nsv5698873mobile element insertion1nstd211human GRCh38 chr19: 32,359,390-32,359,390 , GRCh37.p13 chr19: 32,850,296-32,850,296 ZNF507
    nsv5517906copy number variation1nstd206human GRCh38 chr19: 32,355,523-32,355,594 , GRCh37.p13 chr19: 32,846,429-32,846,500 ZNF507
    nsv5427875mobile element insertion1nstd206human GRCh38 chr19: 32,350,626-32,350,626 , GRCh37.p13 chr19: 32,841,532-32,841,532 ZNF507
    nsv5415742mobile element insertion1nstd206human GRCh38 chr19: 32,359,390-32,359,441 , GRCh37.p13 chr19: 32,850,296-32,850,347 ZNF507
    nsv5024534copy number variation1nstd200human GRCh38 chr19: 32,387,411-32,388,275 , GRCh37.p13 chr19: 32,878,317-32,879,181 DPY19L3-DT, ZNF507
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv4715921copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,022,201 , GRCh38.p12 chr19: 31,654,545-32,531,295 , DPY19L3, 12 more genes
    nsv4712385copy number variation1nstd195human GRCh37 chr19: 32,145,451-33,078,501 , GRCh38.p12 chr19: 31,654,545-32,587,595 , DPY19L3-DT, 13 more genes
    nsv4513933mobile element insertion1nstd166human GRCh37.p13 chr19: 32,841,527-32,841,527 , GRCh38.p12 chr19: 32,350,621-32,350,621 ZNF507
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4365060copy number variation1nstd173human GRCh37 chr19: 32,803,285-33,026,305 , GRCh38.p12 chr19: 32,312,379-32,535,399 ZNF507, DPY19L3-DT, 1 more genes
    nsv4263646copy number variation1nstd166human GRCh37.p13 chr19: 32,841,375-32,841,667 , GRCh38.p12 chr19: 32,350,469-32,350,761 ZNF507
    nsv4257989copy number variation1nstd166human GRCh37.p13 chr19: 32,877,211-32,889,895 , GRCh38.p12 chr19: 32,386,305-32,398,989 DPY19L3-DT, ZNF507
    nsv4254951copy number variation1nstd166human GRCh37.p13 chr19: 32,834,529-32,854,293 , GRCh38.p12 chr19: 32,343,623-32,363,387 ZNF507
    nsv4253157copy number variation1nstd166human GRCh37.p13 chr19: 32,846,560-32,846,625 , GRCh38.p12 chr19: 32,355,654-32,355,719 ZNF507
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
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