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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5515557copy number variation1nstd206human GRCh38 chr19: 51,768,552-52,114,487 , GRCh37.p13 chr19: 52,271,805-52,617,740 ZNF613, ZNF350-AS1, 17 more genes
    nsv5325855copy number variation1nstd204human GRCh37.p13 chr19: 52,640,461-52,676,125 , GRCh38.p13 chr19: 52,137,208-52,172,872 ZNF616, ZNF836, 1 more genes
    nsv5295693copy number variation1nstd204human GRCh38.p13 chr19: 52,136,978-52,165,465 , GRCh37.p13 chr19: 52,640,231-52,668,718 RPL37P23, ZNF616, 1 more genes
    nsv5294291copy number variation1nstd204human GRCh38.p13 chr19: 52,063,101-52,358,000 , GRCh37.p13 chr19: 52,566,354-52,861,253 PPP2R1A, MIR643, 12 more genes
    nsv5288905copy number variation1nstd204human GRCh38.p13 chr19: 52,137,201-52,172,900 , GRCh37.p13 chr19: 52,640,454-52,676,153 RPL37P23, ZNF616, 1 more genes
    nsv5286960copy number variation1nstd204human GRCh38.p13 chr19: 52,137,128-52,152,225 , GRCh37.p13 chr19: 52,640,381-52,655,478 ZNF616, ZNF836, 1 more genes
    nsv5024851copy number variation1nstd200human GRCh38 chr19: 52,106,311-52,273,340 , GRCh37.p13 chr19: 52,609,564-52,776,593 RPL37P23, ZNF766, 7 more genes
    nsv5024847copy number variation1nstd200human GRCh38 chr19: 51,768,552-52,114,487 , GRCh37.p13 chr19: 52,271,805-52,617,740 ZNF615, ZNF649-AS1, 17 more genes
    nsv5021131copy number variation1nstd200human GRCh38 chr19: 52,137,233-52,172,845 , GRCh37.p13 chr19: 52,640,486-52,676,098 ZNF836, RPL37P23, 1 more genes
    nsv5021130copy number variation1nstd200human GRCh38 chr19: 52,133,996-52,137,025 , GRCh37.p13 chr19: 52,637,249-52,640,278 ZNF616
    nsv5021129copy number variation1nstd200human GRCh38 chr19: 52,113,540-52,114,263 , GRCh37.p13 chr19: 52,616,793-52,617,516 ZNF616
    nsv4865280copy number variation1nstd200human GRCh37 chr19: 52,271,805-52,617,740 , GRCh38.p12 chr19: 51,768,552-52,114,487 ZNF649, VN1R98P, 17 more genes
    nsv4853444copy number variation1nstd200human GRCh37 chr19: 52,640,486-52,676,098 , GRCh38.p12 chr19: 52,137,233-52,172,845 ZNF836, RPL37P23, 1 more genes
    nsv4853443copy number variation1nstd200human GRCh37 chr19: 52,616,793-52,617,516 , GRCh38.p12 chr19: 52,113,540-52,114,263 ZNF616
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4705870copy number variation1nstd195human GRCh37 chr19: 52,560,951-52,977,551 , GRCh38.p12 chr19: 52,057,698-52,474,298 ZNF528, ZNF480, 20 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4680470copy number variation1nstd189human GRCh37.p13 chr19: 52,276,523-52,620,956 , GRCh38.p12 chr19: 51,773,270-52,117,703 FPR3, ZNF432, 16 more genes
    nsv4680444copy number variation1nstd189human GRCh37.p13 chr19: 52,271,533-52,617,333 , GRCh38.p12 chr19: 51,768,280-52,114,080 FPR2, FPR3, 17 more genes
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