dbVar for Gene (Select 521) - 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
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
nsv5381786	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 374,557-745,174 , GRCh38.p12 chr4: 380,768-751,386	LOC100533735, ZNF141, 14 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
nsv5223166	copy number variation	1	nstd204	human		GRCh38.p13 chr4: 637,201-1,087,400 , GRCh37.p13 chr4: 630,990-1,081,188	, SLC26A1, 19 more genes
nsv4925133	copy number variation	1	nstd200	human		GRCh38 chr4: 674,448-685,230 , GRCh37.p13 chr4: 668,237-679,019	MYL5, SLC49A3, 1 more genes
nsv4925131	copy number variation	1	nstd200	human		GRCh38 chr4: 644,363-678,091 , GRCh37.p13 chr4: 638,152-671,880	SLC49A3, ATP5ME, 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
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
nsv4729233	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 312,744-694,965 , GRCh38.p12 chr4: 318,955-701,176	TMEM271, ZNF519P4, 13 more genes
nsv4729147	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 68,345-1,109,959 , GRCh38.p12 chr4: 68,453-1,116,171	PCGF3-AS1, LOC105374339, 39 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 302

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Number of Variants: 20

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