dbVar for Gene (Select 1287) - 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
nsv7137063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409	RN7SL581P, HMGB1P32, 2151 more genes
nsv7098723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,681,152-107,783,055 , GRCh38.p12 chrX: 108,437,922-108,539,825	COL4A5, COL4A6
nsv7098490	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,920,710-107,930,944 , GRCh38.p12 chrX: 108,677,480-108,687,714	COL4A5
nsv7098489	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,858,121-107,979,574 , GRCh38.p12 chrX: 108,614,891-108,736,344	IRS4-AS1, IRS4, 1 more genes
nsv7098488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,849,932-107,858,274 , GRCh38.p12 chrX: 108,606,702-108,615,044	COL4A5
nsv7098487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,834,471-107,835,925 , GRCh38.p12 chrX: 108,591,241-108,592,695	COL4A5
nsv7098486	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,807,092-107,898,707 , GRCh38.p12 chrX: 108,563,862-108,655,477	COL4A5
nsv7098485	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,802,274-107,933,678 , GRCh38.p12 chrX: 108,559,044-108,690,448	COL4A5
nsv7098484	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 107,682,568-107,683,456 , GRCh38.p12 chrX: 108,439,338-108,440,226	COL4A5, COL4A6
nsv7098213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,898,541-107,979,574 , GRCh38.p12 chrX: 108,655,311-108,736,344	COL4A5, IRS4, 1 more genes
nsv7098212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,819,120-107,827,775 , GRCh38.p12 chrX: 108,575,890-108,584,545	COL4A5
nsv7098211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,817,240-107,821,596 , GRCh38.p12 chrX: 108,574,010-108,578,366	COL4A5
nsv7098210	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 107,400,230-107,939,608 , GRCh38.p12 chrX: 108,157,000-108,696,378	COL4A6, COL4A5
nsv7098109	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 107,819,120-107,820,077 , GRCh38.p12 chrX: 108,575,890-108,576,847	COL4A5
nsv7098107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020	VSIG1, NXT2, 32 more genes
nsv7097979	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 107,930,692-107,930,944 , GRCh38.p12 chrX: 108,687,462-108,687,714	COL4A5
nsv7097978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,908,717-107,911,754 , GRCh38.p12 chrX: 108,665,487-108,668,524	COL4A5
nsv7097977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 107,867,446-107,869,599 , GRCh38.p12 chrX: 108,624,216-108,626,369	COL4A5
nsv7097976	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 107,782,956-107,898,707 , GRCh38.p12 chrX: 108,539,726-108,655,477	COL4A5
nsv7093340	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 107,841,959-107,842,012 , GRCh38 chrX: 108,598,729-108,598,782	COL4A5

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Result Filters

Object Type

Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 582

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Number of Variants: 20

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