dbVar for Gene (Select 170960) - 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
nsv6112761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973	LOC101928306, PDE6B-AS1, 460 more genes
nsv6112747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372	GPR78, LOC105374510, 362 more genes
nsv5901310	copy number variation	1	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 411,820-457,114 , GRCh38 chr4: 421,820-467,114 , GRCh37.p13 chr4: 415,609-460,865	ABCA11P, ZNF721, 1 more genes
nsv5898862	copy number variation	1	nstd209	human		GRCh38 chr4: 470,275-471,280 , GRCh37.p13 chr4: 464,064-465,069 , GRCh37.p13 chr4\|NW_004775427.1: 460,275-461,280	ZNF721, ABCA11P
nsv5896645	copy number variation	1	nstd209	human		GRCh38 chr4: 450,167-450,269 , GRCh37.p13 chr4\|NW_004775427.1: 440,167-440,269 , GRCh37.p13 chr4: 443,956-444,058	ABCA11P, ZNF721
nsv5894496	copy number variation	1	nstd209	human		GRCh38 chr4: 489,176-489,262 , GRCh37.p13 chr4\|NW_004775427.1: 479,176-479,262 , GRCh37.p13 chr4: 482,965-483,051	ZNF721
nsv5890179	copy number variation	1	nstd209	human		GRCh38 chr4: 497,652-497,969 , GRCh37.p13 chr4\|NW_004775427.1: 487,652-487,969 , GRCh37.p13 chr4: 491,441-491,758	ZNF721, PIGG
nsv5889530	copy number variation	1	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 339,550-470,119 , GRCh38 chr4: 349,550-480,119 , GRCh37.p13 chr4: 343,339-473,908	ZNF141, ABCA11P, 5 more genes
nsv5888439	copy number variation	1	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 405,188-496,542 , GRCh38 chr4: 415,188-506,542 , GRCh37.p13 chr4: 408,977-500,331	PIGG, LOC100533734, 3 more genes
nsv5839658	copy number variation	1	nstd209	human		GRCh38 chr4: 495,909-535,996 , GRCh37.p13 chr4: 507,005-529,785	PIGG, ZNF721
nsv5839628	copy number variation	2	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 411,789-428,928 , GRCh38 chr4: 421,789-438,928 , GRCh37.p13 chr4: 415,578-432,717	ZNF721, LOC100533734, 1 more genes
nsv5839589	copy number variation	2	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 421,641-428,928 , GRCh38 chr4: 431,641-438,928 , GRCh37.p13 chr4: 425,430-432,717	ZNF721, LOC100533734, 1 more genes
nsv5839343	copy number variation	1	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 458,182-502,569 , GRCh38 chr4: 468,182-512,569 , GRCh37.p13 chr4: 461,971-506,358	ABCA11P, ZNF721, 2 more genes
nsv5839341	copy number variation	2	nstd209	human		GRCh37.p13 chr4\|NW_004775427.1: 456,032-464,336 , GRCh38 chr4: 466,032-474,336 , GRCh37.p13 chr4: 459,821-468,125	ZNF721, ABCA11P, 1 more genes
nsv5729986	mobile element insertion	1	nstd211	human		GRCh38 chr4: 471,108-471,108 , GRCh37.p13 chr4\|NW_004775427.1: 461,108-461,108 , GRCh37.p13 chr4: 464,897-464,897	ZNF721, ABCA11P
nsv5719652	mobile element insertion	1	nstd211	human		GRCh38 chr4: 471,093-471,093 , GRCh37.p13 chr4: 464,882-464,882 , GRCh37.p13 chr4\|NW_004775427.1: 461,093-461,093	ABCA11P, ZNF721
nsv5690586	mobile element insertion	1	nstd211	human		GRCh38 chr4: 495,311-495,311 , GRCh37.p13 chr4\|NW_004775427.1: 485,311-485,311 , GRCh37.p13 chr4: 489,100-489,100	ZNF721
nsv5673651	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,125-998,181 , GRCh38.p12 chr4: 499,336-1,004,393	ATP5ME, PDE6B, 19 more genes
nsv5673565	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 1-705,161 , GRCh37.p13 chr4\|NW_004775427.1: 1-503,215 , GRCh37.p13 chr4: 10,001-507,004	ABCA11P, LOC105374377, 23 more genes
nsv5564485	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 264,888-682,916 , GRCh38.p12 chr4: 271,099-689,127	TMEM271, PDE6B, 15 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

Links from Gene

Items: 1 to 20 of 513

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Number of Variants: 20

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