nox5[All Fields] AND 1[has_clinical] - 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
nsv3918098	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 66,931,182-67,077,978 , GRCh37.p13 chr15: 69,144,128-69,290,924 , GRCh38.p12 chr15: 68,851,789-68,998,585	NOX5, SPESP1
nsv6637908	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 69,255,715-69,347,081 , GRCh38.p12 chr15: 68,963,376-69,054,741	NOX5, LOC100422194
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	NOX5, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	NOX5, RNU6-18P, 1442 more genes
nsv3920633	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678	NOX5, NEO1, 95 more genes
nsv4456268	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 67,369,118-70,481,307 , GRCh38.p12 chr15: 67,076,780-70,188,968	NOX5, ANP32A-IT1, 48 more genes
nsv3914011	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 65,273,973-67,165,679 , GRCh37 chr15: 67,486,919-69,378,625 , GRCh38 chr15: 67,194,581-69,086,285	NOX5, LOC105370871, 29 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	NOX5, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	NOX5, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	NOX5, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	NOX5, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	NOX5, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	NOX5, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	NOX5, CILP, 1176 more genes
nsv3917589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724	NOX5, GAPDHP61, 840 more genes
nsv3895615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 64,637,227-102,509,910 , GRCh38.p12 chr15: 64,345,028-101,969,707	NOX5, KRT18P47, 781 more genes
nsv7098897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098	NOX5, LINC00933, 540 more genes
nsv3905308	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685	NOX5, ACAN, 861 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	NOX5, SNRPCP18, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	NOX5, SNORD116-23, 1622 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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