dbVar for Gene (Select 54872) - 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
nsv7097254	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 514,825-533,158 , GRCh38.p12 chr4: 521,036-539,369	PIGG
nsv7097253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 509,742-533,158 , GRCh38.p12 chr4: 515,953-539,369	PIGG
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
nsv7096857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 532,922-533,158 , GRCh38.p12 chr4: 539,133-539,369	PIGG
nsv7096855	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 524,205-533,158 , GRCh38.p12 chr4: 530,416-539,369	PIGG
nsv7096854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 524,205-527,790 , GRCh38.p12 chr4: 530,416-534,001	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
nsv7096733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 520,808-1,020,391 , GRCh38.p12 chr4: 527,019-1,026,603	PDE6B-AS1, PIGG, 19 more genes
nsv7096732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 501,174-533,158 , GRCh38.p12 chr4: 507,385-539,369	PIGG
nsv7096731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 494,165-494,410 , GRCh38.p12 chr4: 500,376-500,621	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
nsv6736971	copy number variation	1	nstd229	human		GRCh38 chr4: 528,623-536,829 , GRCh37.p13 chr4: 522,412-530,618	PIGG
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

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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 480

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Number of Variants: 20

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