dbVar for Gene (Select 10608) - 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
nsv5673743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513	ZFYVE28, LINC01587, 81 more genes
nsv5381775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653	RN7SL671P, HTT-AS, 96 more genes
nsv4761770	inversion	1	nstd199	human		GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093	, ADD1, 2433 more genes
nsv4758212	inversion	1	nstd199	human		GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290	, ADD1, 2433 more genes
nsv4754592	inversion	1	nstd199	human		GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182	, ADD1, 2433 more genes
nsv4753570	inversion	1	nstd199	human		GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259	, ADD1, 2434 more genes
nsv4751554	inversion	1	nstd199	human		GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630	, ADD1, 2434 more genes
nsv4729500	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-2,503,033 , GRCh38.p12 chr4: 68,453-2,501,306	MIR4800, NELFA, 80 more genes
nsv4729295	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-5,831,521 , GRCh38.p12 chr4: 68,453-5,829,794	FGFR3, NICOL1, 151 more genes
nsv4729016	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-5,046,326 , GRCh38.p12 chr4: 68,453-5,044,599	TMEM175, LOC105374346, 145 more genes
nsv4728907	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1,941,633-3,879,802 , GRCh38.p12 chr4: 1,939,906-3,878,075	FAM193A, SCARNA22, 46 more genes
nsv4684161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881	TLR10, WDR1, 669 more genes
nsv4681037	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 2,061,219-2,835,581 , GRCh38.p12 chr4: 2,059,492-2,833,854	MXD4, LOC105374353, 18 more genes
nsv4674477	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-2,786,584 , GRCh38.p12 chr4: 68,453-2,784,857	UVSSA, LOC100130872, 83 more genes
nsv4674429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-6,984,507 , GRCh38.p12 chr4: 68,453-6,982,780	STX18-IT1, SLC26A1, 170 more genes
nsv4674378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859	USP17L30, LOC100422637, 394 more genes
nsv4674283	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-9,768,141 , GRCh38.p12 chr4: 68,453-9,766,517	MFSD10, PCGF3-AS1, 255 more genes
nsv4674174	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-10,312,798 , GRCh38.p12 chr4: 68,453-10,311,174	RNA5SP153, NICOL1, 267 more genes

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Number of Variants: 20

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Result Filters

Object Type

Organism

Variant Type

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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 463

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Number of Variants: 20

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