egfr[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
nsv7097379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 55,223,561-55,233,842 , GRCh38.p12 chr7: 55,155,868-55,166,149	EGFR
nsv6312545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 55,221,694-55,225,456 , GRCh38.p12 chr7: 55,154,001-55,157,763	EGFR
nsv3891050	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,128,731-55,135,681 , GRCh38.p12 chr7: 55,061,038-55,067,988	EGFR
nsv3899602	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,355-55,238,268 , GRCh38.p12 chr7: 55,166,662-55,170,575	EGFR
nsv3903828	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,355-55,237,283 , GRCh38.p12 chr7: 55,166,662-55,169,590	EGFR
nsv3895719	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,355-55,236,774 , GRCh38.p12 chr7: 55,166,662-55,169,081	EGFR
nsv3891746	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,565-55,236,774 , GRCh38.p12 chr7: 55,166,872-55,169,081	EGFR
nsv3891098	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,134,272-55,135,681 , GRCh38.p12 chr7: 55,066,579-55,067,988	EGFR
nsv6634667	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 55,134,860-55,135,857 , GRCh38 chr7: 55,067,167-55,068,164	EGFR
nsv3900804	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,355-55,235,288 , GRCh38.p12 chr7: 55,166,662-55,167,595	EGFR
nsv3893205	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 55,234,682-55,234,857 , GRCh38.p12 chr7: 55,166,989-55,167,164	EGFR
nsv5381470	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,209,969-55,223,649 , GRCh38.p12 chr7: 55,142,276-55,155,956	EGFR
nsv4681308	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,227,822-55,229,334 , GRCh38.p12 chr7: 55,160,129-55,161,641	EGFR
nsv4682496	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,272,939-55,274,084 , GRCh38.p12 chr7: 55,205,246-55,206,391	EGFR
nsv7097632	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,214,289-55,214,443 , GRCh38.p12 chr7: 55,146,596-55,146,750	EGFR
nsv4578382	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 55,174,831-55,174,966 , GRCh37 chr7: 55,242,525-55,242,660	EGFR
nsv4578371	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,259,446-55,259,533 , GRCh38 chr7: 55,191,748-55,191,835	EGFR
nsv5564473	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,259,402-55,274,084 , GRCh38.p12 chr7: 55,191,709-55,206,391	EGFR
nsv4683301	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,086,971-55,219,065 , GRCh38.p12 chr7: 55,019,278-55,151,372	EGFR, LOC105375284
nsv5381723	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 55,209,969-55,274,084 , GRCh38.p12 chr7: 55,142,276-55,206,391	EGFR, EGFR-AS1

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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 153

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Number of Variants: 20

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