ctnna1[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
nsv6314734	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 138,782,925-138,783,171 , GRCh37 chr5: 138,118,614-138,118,860	CTNNA1
nsv7093357	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr5: 138,930,659-138,930,718 , GRCh37 chr5: 138,266,348-138,266,407	CTNNA1
nsv4683036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,240,028-138,269,778 , GRCh38.p12 chr5: 138,904,339-138,934,089	CTNNA1
nsv7096753	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,117,614-138,145,913 , GRCh38.p12 chr5: 138,781,925-138,810,224	CTNNA1
nsv4683427	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,145,717-138,163,417 , GRCh38.p12 chr5: 138,810,028-138,827,728	CTNNA1
nsv7097023	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,253,411-138,269,778 , GRCh38.p12 chr5: 138,917,722-138,934,089	CTNNA1
nsv7097121	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,240,028-138,253,597 , GRCh38.p12 chr5: 138,904,339-138,917,908	CTNNA1
nsv7096756	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,260,189-138,269,778 , GRCh38.p12 chr5: 138,924,500-138,934,089	CTNNA1
nsv7097122	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,266,509-138,268,411 , GRCh38.p12 chr5: 138,930,820-138,932,722	CTNNA1
nsv7097510	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,269,481-138,269,778 , GRCh38.p12 chr5: 138,933,792-138,934,089	CTNNA1
nsv6636183	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,111,845-138,112,038 , GRCh38 chr5: 138,776,156-138,776,349	CTNNA1
nsv5564198	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,253,421-138,253,597 , GRCh38.p12 chr5: 138,917,732-138,917,908	CTNNA1
nsv7097120	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,147,862-138,148,001 , GRCh38.p12 chr5: 138,812,173-138,812,312	CTNNA1
nsv6312177	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,117,614-138,117,728 , GRCh38.p12 chr5: 138,781,925-138,782,039	CTNNA1
nsv6312267	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,163,377-138,163,448 , GRCh38 chr5: 138,827,688-138,827,759	CTNNA1
nsv7097508	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,117,614-138,160,508 , GRCh38.p12 chr5: 138,781,925-138,824,819	CTNNA1
nsv7097118	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,117,614-138,148,001 , GRCh38.p12 chr5: 138,781,925-138,812,312	CTNNA1
nsv4452989	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr5: 138,781,915-138,810,214 , GRCh37 chr5: 138,117,604-138,145,903	CTNNA1
nsv5381512	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,117,614-138,145,893 , GRCh38.p12 chr5: 138,781,925-138,810,204	CTNNA1
nsv7096755	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 138,253,421-138,269,778 , GRCh38.p12 chr5: 138,917,732-138,934,089	CTNNA1

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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 60

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Number of Variants: 20

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Supplemental Content

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