dbVar for Gene (Select 7157) - 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
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	RFLNB, C17orf100, 401 more genes
nsv7143101	copy number variation	1	nstd232	human		GRCh37.p13 chr17: 7,578,287-7,578,367 , GRCh38.p12 chr17: 7,674,969-7,675,049	TP53
nsv7141433	copy number variation	1	nstd232	human		GRCh37.p13 chr17: 7,576,926-7,577,017 , GRCh38.p12 chr17: 7,673,608-7,673,699	TP53
nsv7137330	insertion	1	nstd232	human		GRCh37.p13 chr17: 7,579,593-7,579,593 , GRCh38.p12 chr17: 7,676,275-7,676,275	TP53
nsv7098895	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471	LOC105371512, EIF4A1, 61 more genes
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	TP53, WRAP53
nsv7098755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,574,126-7,586,609 , GRCh38.p12 chr17: 7,670,808-7,683,291	TP53
nsv7095414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936	CTC1, SAT2, 103 more genes
nsv7095413	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,123,304-7,606,804 , GRCh38.p12 chr17: 7,219,985-7,703,486	MPDU1, PLSCR3, 50 more genes
nsv7095410	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr17: 6,328,780-7,606,804 , GRCh38.p12 chr17: 6,425,460-7,703,486	PITPNM3, SLC2A4, 85 more genes
nsv7095366	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,578,129-7,606,804 , GRCh38.p12 chr17: 7,674,811-7,703,486	EFNB3, TP53, 1 more genes
nsv7095365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310	TRK-TTT3-5, WRAP53, 59 more genes
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
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	TP53, WRAP53
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
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
nsv7094915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105	MIR324, SLC2A4, 101 more genes
nsv7093482	delins	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,577,002-7,577,004 , GRCh38 chr17: 7,673,684-7,673,686	TP53
nsv7093239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,578,823-7,579,404 , GRCh38 chr17: 7,675,505-7,676,086	TP53
nsv7093097	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 7,674,872-7,674,873 , GRCh37 chr17: 7,578,190-7,578,191	TP53

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Result Filters

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 280

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Number of Variants: 20

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