dbVar for Gene (Select 2261) - 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
nsv5673649	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1,619,775-2,181,192 , GRCh38.p12 chr4: 1,618,048-2,179,465	NSD2, TMEM129, 15 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
nsv4928485	copy number variation	1	nstd200	human		GRCh38 chr4: 1,808,240-1,861,252 , GRCh37.p13 chr4: 1,809,967-1,862,979	LETM1, FGFR3
nsv4925160	copy number variation	1	nstd200	human		GRCh38 chr4: 1,714,954-1,798,100 , GRCh37.p13 chr4: 1,716,681-1,799,827	FGFR3, TACC3, 3 more genes
nsv4805179	copy number variation	1	nstd200	human		GRCh37 chr4: 1,716,681-1,799,827 , GRCh38.p12 chr4: 1,714,954-1,798,100	SLBP, LOC112268460, 3 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
nsv4729620	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr4: 1,427,160-1,835,067 , GRCh37 chr4: 1,420,948-1,836,794	FGFR3, LETM1, 7 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
nsv4729483	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-2,137,211 , GRCh38.p12 chr4: 68,453-2,135,484	LOC105374348, ZNF721, 67 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
nsv4728898	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,778,534-1,912,732 , GRCh38.p12 chr4: 1,776,807-1,911,005	NSD2, FGFR3, 2 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
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

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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

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Study Type

Subject Phenotype Status

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Items: 1 to 20 of 385

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Number of Variants: 20

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