wrap53[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
nsv4682576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-7,606,455 , GRCh38.p12 chr17: 7,668,434-7,703,137	WRAP53, TP53
nsv7094989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-7,593,029 , GRCh38.p12 chr17: 7,668,434-7,689,711	WRAP53, TP53
nsv6310411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-7,591,611 , GRCh38.p12 chr17: 7,668,434-7,688,293	WRAP53, TP53
nsv3877485	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 7,668,402-7,687,550 , GRCh37 chr17: 7,571,720-7,590,868	WRAP53, TP53
nsv5672893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,572,921-7,591,661 , GRCh38.p12 chr17: 7,669,603-7,688,343	WRAP53, TP53
nsv4450650	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,572,917-7,591,611 , GRCh38 chr17: 7,669,599-7,688,293	WRAP53, TP53
nsv7094919	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,572,921-7,591,611 , GRCh38.p12 chr17: 7,669,603-7,688,293	WRAP53, TP53
nsv5381255	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr17: 7,576,843-7,593,029 , GRCh38.p12 chr17: 7,673,525-7,689,711	WRAP53, TP53
nsv7094990	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,589,449-7,593,039 , GRCh38.p12 chr17: 7,686,131-7,689,721	WRAP53, TP53
nsv4683659	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,589,449-7,593,029 , GRCh38.p12 chr17: 7,686,131-7,689,711	WRAP53, TP53
nsv4450549	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,590,924-7,591,611 , GRCh38 chr17: 7,687,606-7,688,293	WRAP53, TP53
nsv997029	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr17: 7,571,720-7,590,868 , GRCh38.p12 chr17: 7,668,402-7,687,550	WRAP53, TP53
nsv5381040	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr17: 7,578,129-7,593,029 , GRCh38.p12 chr17: 7,674,811-7,689,711	WRAP53, TP53
nsv5381041	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr17: 7,589,449-7,591,611 , GRCh38.p12 chr17: 7,686,131-7,688,293	WRAP53, TP53
nsv7098770	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 7,584,834-7,594,887 , GRCh38.p12 chr17: 7,681,516-7,691,569	WRAP53, TP53
nsv3873759	copy number variation	2	nstd102	human	Uncertain significance, Likely pathogenic	GRCh37 chr17: 7,590,695-7,590,868 , GRCh38 chr17: 7,687,377-7,687,550	WRAP53, TP53
nsv7094920	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,590,130-7,598,840 , GRCh38.p12 chr17: 7,686,812-7,695,522	WRAP53, TP53
nsv6310198	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,590,929-7,599,621 , GRCh38.p12 chr17: 7,687,611-7,696,303	WRAP53, TP53
nsv4683925	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,572,917-7,591,611 , GRCh38.p12 chr17: 7,669,599-7,688,293	WRAP53, TP53
nsv4453881	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,576,843-7,591,611 , GRCh38 chr17: 7,673,525-7,688,293	WRAP53, TP53

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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 66

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Number of Variants: 20

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