dbVar for Gene (Select 79400) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5937495	copy number variation	1	nstd209	human		GRCh38 chr15: 69,023,704-69,025,354 , GRCh37.p13 chr15: 69,316,044-69,317,694	NOX5, LOC100422194
nsv5847934	copy number variation	1	nstd209	human		GRCh38 chr15: 69,023,681-69,025,980 , GRCh37.p13 chr15: 69,316,021-69,318,320	LOC100422194, NOX5
nsv5645452	insertion	1	nstd207	human		GRCh38 chr15: 69,045,556-69,045,556 , GRCh37.p13 chr15: 69,337,896-69,337,896	NOX5
nsv5524290	copy number variation	1	nstd206	human		GRCh38 chr15: 69,023,706-69,025,355 , GRCh37.p13 chr15: 69,316,046-69,317,695	NOX5, LOC100422194
nsv5518711	copy number variation	1	nstd206	human		GRCh38 chr15: 68,988,321-68,996,652 , GRCh37.p13 chr15: 69,280,660-69,288,991	NOX5
nsv5380758	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289	LOC105370794, HNRNPA1P45, 1173 more genes
nsv5349112	translocation	1	nstd200	human		GRCh38 chr15: 69,025,355-69,025,355 , GRCh38 chr15: 69,023,706-69,023,706 , GRCh37.p13 chr15: 69,317,695-69,317,695 , GRCh37.p13 chr15: 69,316,046-69,316,046	NOX5, LOC100422194
nsv5338068	translocation	1	nstd200	human		GRCh37 chr15: 69,316,046-69,316,046 , GRCh37 chr15: 69,317,695-69,317,695 , GRCh38.p12 chr15: 69,023,706-69,023,706 , GRCh38.p12 chr15: 69,025,355-69,025,355	LOC100422194, NOX5
nsv5318770	copy number variation	1	nstd204	human		GRCh37.p13 chr15: 69,316,023-69,317,717 , GRCh38.p13 chr15: 69,023,683-69,025,377	LOC100422194, NOX5
nsv5273503	copy number variation	1	nstd204	human		GRCh38.p13 chr15: 69,023,701-69,024,900 , GRCh37.p13 chr15: 69,316,041-69,317,240	NOX5, LOC100422194
nsv5269782	copy number variation	1	nstd204	human		GRCh38.p13 chr15: 69,023,931-69,025,330 , GRCh37.p13 chr15: 69,316,271-69,317,670	NOX5, LOC100422194
nsv5261752	copy number variation	1	nstd204	human		GRCh38.p13 chr15: 68,819,401-68,984,500 , GRCh37.p13 chr15: 69,111,740-69,276,839	NOX5, ANP32A, 2 more genes
nsv5157957	mobile element insertion	1	nstd203	human		GRCh38 chr15: 68,950,212-68,950,236 , GRCh37.p13 chr15: 69,242,551-69,242,575	NOX5
nsv5155284	mobile element insertion	1	nstd203	human		GRCh38 chr15: 68,937,134-68,937,150 , GRCh37.p13 chr15: 69,229,473-69,229,489	NOX5, SPESP1
nsv5141944	mobile element insertion	1	nstd203	human		GRCh38 chr15: 68,963,601-68,963,614 , GRCh37.p13 chr15: 69,255,940-69,255,953	NOX5
nsv5005537	copy number variation	1	nstd200	human		GRCh38 chr15: 68,782,548-69,149,608 , GRCh37.p13 chr15: 69,074,887-69,441,947	NOX5, EWSAT1, 6 more genes
nsv4992183	copy number variation	1	nstd200	human		GRCh38 chr15: 69,050,958-69,059,104 , GRCh37.p13 chr15: 69,343,298-69,351,444	NOX5
nsv4992182	copy number variation	1	nstd200	human		GRCh38 chr15: 68,988,452-68,996,652 , GRCh37.p13 chr15: 69,280,791-69,288,991	NOX5
nsv4992181	copy number variation	1	nstd200	human		GRCh38 chr15: 68,977,510-68,978,353 , GRCh37.p13 chr15: 69,269,849-69,270,692	NOX5
nsv4992180	copy number variation	1	nstd200	human		GRCh38 chr15: 68,963,776-68,971,383 , GRCh37.p13 chr15: 69,256,115-69,263,722	NOX5

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 277

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Number of Variants: 20

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