smad4[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
nsv4683051	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,556,291-48,604,847 , GRCh38.p12 chr18: 51,029,921-51,078,477	SMAD4
nsv4681697	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr18: 48,556,583-48,604,837 , GRCh38.p12 chr18: 51,030,213-51,078,467	SMAD4
nsv3878853	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 51,030,213-51,065,606 , GRCh37 chr18: 48,556,583-48,591,976	SMAD4
nsv3885728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,573,411-48,604,843 , GRCh38.p12 chr18: 51,047,041-51,078,473	SMAD4
nsv3871555	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,593,389-48,611,412 , GRCh38 chr18: 51,067,019-51,085,042	SMAD4
nsv5673142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,593,383-48,604,842 , GRCh38.p12 chr18: 51,067,013-51,078,472	SMAD4
nsv4769319	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,595,259-48,604,741 , GRCh38 chr18: 51,068,889-51,078,371	SMAD4
nsv7095384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,602,988-48,604,837 , GRCh38.p12 chr18: 51,076,618-51,078,467	SMAD4
nsv3871785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,602,998-48,604,847 , GRCh38 chr18: 51,076,628-51,078,477	SMAD4
nsv6310213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,602,998-48,604,837 , GRCh38.p12 chr18: 51,076,628-51,078,467	SMAD4
nsv7095250	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,591,783-48,593,567 , GRCh38.p12 chr18: 51,065,413-51,067,197	SMAD4
nsv3871006	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr18: 48,591,787-48,593,563 , GRCh38 chr18: 51,065,417-51,067,193	SMAD4
nsv6310264	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 48,591,783-48,591,986 , GRCh38.p12 chr18: 51,065,413-51,065,616	SMAD4
nsv3878726	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr18: 48,556,583-48,604,847 , GRCh38 chr18: 51,030,213-51,078,477	SMAD4
nsv5673061	copy number variation	2	nstd102	human	Pathogenic, Likely benign	GRCh37 chr18: 48,604,616-48,604,837 , GRCh38.p12 chr18: 51,078,246-51,078,467	SMAD4
nsv7093172	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr18: 48,556,994-48,573,471 , GRCh38.p12 chr18: 51,030,624-51,047,101	SMAD4
nsv5672898	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 48,573,411-48,604,842 , GRCh38.p12 chr18: 51,047,041-51,078,472	SMAD4
nsv7095446	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 48,573,397-48,573,685 , GRCh38.p12 chr18: 51,047,027-51,047,315	SMAD4
nsv5673060	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 48,573,407-48,573,675 , GRCh38.p12 chr18: 51,047,037-51,047,305	SMAD4
nsv1398545	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr18: 48,573,416-48,573,665 , GRCh38 chr18: 51,047,046-51,047,295	SMAD4

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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 73

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Number of Variants: 20

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Supplemental Content

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