pigg[All Fields] AND 1[has_clinical] - 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
nsv7096732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 501,174-533,158 , GRCh38.p12 chr4: 507,385-539,369	PIGG
nsv7097253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 509,742-533,158 , GRCh38.p12 chr4: 515,953-539,369	PIGG
nsv6311836	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 502,598-509,994 , GRCh38.p12 chr4: 508,809-516,205	PIGG
nsv6314976	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 512,202-518,547 , GRCh38 chr4: 518,413-524,758	PIGG
nsv6314984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,968-499,930 , GRCh38 chr4: 500,179-506,141	PIGG
nsv7096854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 524,205-527,790 , GRCh38.p12 chr4: 530,416-534,001	PIGG
nsv7096731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 494,165-494,410 , GRCh38.p12 chr4: 500,376-500,621	PIGG
nsv6314972	delins	1	nstd102	human	Pathogenic	GRCh37 chr4: 499,456-499,529 , GRCh38 chr4: 505,667-505,740	PIGG
nsv6137839	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 499,507-502,759 , GRCh38.p12 chr4: 505,718-508,970	PIGG
nsv5381603	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 527,587-533,178 , GRCh38.p12 chr4: 533,798-539,389	PIGG
nsv7096857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 532,922-533,158 , GRCh38.p12 chr4: 539,133-539,369	PIGG
nsv7097254	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 514,825-533,158 , GRCh38.p12 chr4: 521,036-539,369	PIGG
nsv7096855	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 524,205-533,158 , GRCh38.p12 chr4: 530,416-539,369	PIGG
nsv3882460	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr4: 493,105-533,178 , GRCh38.p12 chr4: 499,316-539,389	PIGG, ZNF721
nsv7096997	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-517,722 , GRCh38.p12 chr4: 499,336-523,933	PIGG, ZNF721
nsv3877345	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,105-502,779 , GRCh38.p12 chr4: 499,316-508,990	PIGG, ZNF721
nsv3889671	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,105-499,736 , GRCh38.p12 chr4: 499,316-505,947	PIGG, ZNF721
nsv7096853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-499,736 , GRCh38.p12 chr4: 499,336-505,947	PIGG, ZNF721
nsv5381370	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-499,726 , GRCh38.p12 chr4: 499,336-505,937	PIGG, ZNF721
nsv7097252	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,125-663,896 , GRCh38.p12 chr4: 499,336-670,107	PIGG, PDE6B, 4 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

Search results

Items: 1 to 20 of 172

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Number of Variants: 20

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