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
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	OR7E84P, FAM193A, 764 more genes
nsv7137196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072	ECM1P2, LOC105378240, 482 more genes
nsv7097252	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,125-663,896 , GRCh38.p12 chr4: 499,336-670,107	PDE6B, PIGG, 4 more genes
nsv7097251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817	PDE6B, LOC105374339, 44 more genes
nsv7096997	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-517,722 , GRCh38.p12 chr4: 499,336-523,933	ZNF721, PIGG
nsv7096853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-499,736 , GRCh38.p12 chr4: 499,336-505,947	ZNF721, PIGG
nsv7054796	inversion	1	nstd229	human		GRCh38 chr4: 464,668-619,396 , GRCh37.p13 chr4: 507,005-613,185	PDE6B, LOC100533735, 5 more genes
nsv7048751	inversion	1	nstd229	human		GRCh38 chr4: 498,657-507,101 , GRCh37.p13 chr4\|NW_004775427.1: 488,657-497,101 , GRCh37.p13 chr4: 492,446-500,890	ZNF721, PIGG
nsv7047958	inversion	1	nstd229	human		GRCh37.p13 chr4\|NW_004775427.1: 368,008-497,813 , GRCh38 chr4: 378,008-507,813 , GRCh37.p13 chr4: 371,797-501,602	ZNF141, ABCA11P, 5 more genes
nsv6736897	copy number variation	1	nstd229	human		GRCh38 chr4: 445,214-450,733 , GRCh37.p13 chr4\|NW_004775427.1: 435,214-440,733 , GRCh37.p13 chr4: 439,003-444,522	ZNF721, ABCA11P
nsv6736833	copy number variation	1	nstd229	human		GRCh37.p13 chr4\|NW_004775427.1: 339,183-503,215 , GRCh38 chr4: 349,183-526,025 , GRCh37.p13 chr4: 342,972-507,004	ZNF141, PIGG, 6 more genes
nsv6736703	copy number variation	1	nstd229	human		GRCh38 chr4: 392,960-701,480 , GRCh37.p13 chr4: 507,005-695,269	PDE6B, SLC49A3, 11 more genes
nsv6736524	copy number variation	1	nstd229	human		GRCh38 chr4: 455,700-463,355 , GRCh37.p13 chr4\|NW_004775427.1: 445,700-453,355 , GRCh37.p13 chr4: 449,489-457,144	ZNF721, ABCA11P
nsv6736195	copy number variation	1	nstd229	human		GRCh38 chr4: 411,490-446,972 , GRCh37.p13 chr4: 405,279-440,761 , GRCh37.p13 chr4\|NW_004775427.1: 401,490-436,972	ZNF721, ABCA11P, 1 more genes
nsv6734975	copy number variation	1	nstd229	human		GRCh38 chr4: 477,346-477,547 , GRCh37.p13 chr4\|NW_004775427.1: 467,346-467,547 , GRCh37.p13 chr4: 471,135-471,336	ZNF721, LOC100533735
nsv6734656	copy number variation	1	nstd229	human		GRCh38 chr4: 252,620-648,835 , GRCh37.p13 chr4\|NW_004775427.1: 242,620-503,215 , GRCh37.p13 chr4: 246,409-507,004	PIGG, ZNF519P4, 13 more genes
nsv6734309	copy number variation	1	nstd229	human		GRCh38 chr4: 355,729-445,313 , GRCh37.p13 chr4: 349,518-439,102 , GRCh37.p13 chr4\|NW_004775427.1: 345,729-435,313	ZNF519P4, LOC100533734, 3 more genes
nsv6732964	copy number variation	1	nstd229	human		GRCh38 chr4: 414,201-439,500 , GRCh37.p13 chr4\|NW_004775427.1: 404,201-429,500 , GRCh37.p13 chr4: 407,990-433,289	ZNF721, ABCA11P, 1 more genes
nsv6732170	copy number variation	1	nstd229	human		GRCh38 chr4: 461,616-476,455 , GRCh37.p13 chr4: 455,405-470,244 , GRCh37.p13 chr4\|NW_004775427.1: 451,616-466,455	LOC100533735, ZNF721, 1 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 596

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Number of Variants: 20

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