dbVar for Gene (Select 5165) - 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
nsv7148140	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035	ARX, LOC107985632, 85 more genes
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
nsv7098367	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 24,512,839-24,767,129 , GRCh38.p12 chrX: 24,494,722-24,749,012	H2BP7, LOC100288233, 6 more genes
nsv7098252	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 24,544,295-24,557,281 , GRCh38.p12 chrX: 24,526,178-24,539,164	PDK3
nsv7098251	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chrX: 24,483,573-25,033,854 , GRCh38.p12 chrX: 24,465,456-25,015,737	PCYT1B-AS1, PCYT1B, 8 more genes
nsv7098017	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 24,549,754-24,549,907 , GRCh38.p12 chrX: 24,531,637-24,531,790	PDK3
nsv7098016	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 24,512,839-25,033,854 , GRCh38.p12 chrX: 24,494,722-25,015,737	EEF1B2P3, PDK3, 8 more genes
nsv7086268	copy number variation	1	nstd229	human		GRCh38 chrX: 24,539,072-24,542,385 , GRCh37.p13 chrX: 24,557,189-24,560,502	PDK3
nsv7086267	copy number variation	1	nstd229	human		GRCh38 chrX: 24,533,160-24,533,477 , GRCh37.p13 chrX: 24,551,277-24,551,594	PDK3
nsv7086266	copy number variation	1	nstd229	human		GRCh38 chrX: 24,530,410-24,543,615 , GRCh37.p13 chrX: 24,548,527-24,561,732	PDK3
nsv7086265	copy number variation	1	nstd229	human		GRCh38 chrX: 24,515,580-24,516,015 , GRCh37.p13 chrX: 24,533,697-24,534,132	PDK3
nsv7086264	copy number variation	1	nstd229	human		GRCh38 chrX: 24,510,942-24,511,224 , GRCh37.p13 chrX: 24,529,059-24,529,341	PDK3
nsv7086263	copy number variation	1	nstd229	human		GRCh38 chrX: 24,487,078-24,487,298 , GRCh37.p13 chrX: 24,505,195-24,505,415	PDK3
nsv7086262	copy number variation	1	nstd229	human		GRCh38 chrX: 24,480,082-24,891,387 , GRCh37.p13 chrX: 24,498,199-24,909,504	PCYT1B-AS1, PCYT1B, 7 more genes
nsv7086261	copy number variation	1	nstd229	human		GRCh38 chrX: 24,475,019-24,869,033 , GRCh37.p13 chrX: 24,493,136-24,887,150	SNRPEP9, POLA1, 7 more genes
nsv7086260	copy number variation	1	nstd229	human		GRCh38 chrX: 24,465,556-24,559,057 , GRCh37.p13 chrX: 24,483,673-24,577,174	SNRPEP9, PDK3, 1 more genes
nsv7086259	copy number variation	1	nstd229	human		GRCh38 chrX: 24,464,017-24,547,873 , GRCh37.p13 chrX: 24,482,134-24,565,990	PDK3, SNRPEP9
nsv7086256	copy number variation	1	nstd229	human		GRCh38 chrX: 24,445,701-24,706,000 , GRCh37.p13 chrX: 24,463,818-24,724,117	POLA1, SNRPEP9, 5 more genes
nsv7086252	copy number variation	1	nstd229	human		GRCh38 chrX: 24,357,128-25,105,439 , GRCh37.p13 chrX: 24,375,245-25,123,556	EEF1B2P3, PDK3, 12 more genes
nsv7086247	copy number variation	1	nstd229	human		GRCh38 chrX: 24,287,892-25,219,400 , GRCh37.p13 chrX: 24,306,009-25,237,517	PDK3, EEF1B2P3, 14 more genes

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Number of Variants: 20

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Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

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Items: 1 to 20 of 426

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Number of Variants: 20

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