kcnq1[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
nsv3917867	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 2,454,516-2,461,603 , GRCh37 chr11: 2,475,746-2,482,833 , NCBI36 chr11: 2,432,322-2,439,409	KCNQ1
nsv3886023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,604,645-2,610,104 , GRCh38 chr11: 2,583,415-2,588,874	KCNQ1
nsv4681670	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,604,655-2,610,094 , GRCh38.p12 chr11: 2,583,425-2,588,864	KCNQ1
nsv5672629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,604,665-2,610,084 , GRCh38.p12 chr11: 2,583,435-2,588,854	KCNQ1
nsv5672706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,606,422-2,608,942 , GRCh38.p12 chr11: 2,585,192-2,587,712	KCNQ1
nsv3872493	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,606,442-2,608,922 , GRCh38 chr11: 2,585,212-2,587,692	KCNQ1
nsv3888756	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,591,858-2,594,216 , GRCh38 chr11: 2,570,628-2,572,986	KCNQ1
nsv5672707	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,797,170-2,798,282 , GRCh38.p12 chr11: 2,775,940-2,777,052 , GRCh38.p12 chr11\|NT_187585.1: 8,127-9,239	KCNQ1
nsv4452366	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 2,775,954-2,777,038 , GRCh37 chr11: 2,797,184-2,798,268	KCNQ1
nsv3883088	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 2,775,960-2,777,032 , GRCh37 chr11: 2,797,190-2,798,262	KCNQ1
nsv5672628	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,591,848-2,592,643 , GRCh38.p12 chr11: 2,570,618-2,571,413	KCNQ1
nsv7093844	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,466,329-2,466,734 , GRCh38.p12 chr11: 2,445,099-2,445,504	KCNQ1
nsv4683747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,604,655-2,604,785 , GRCh38.p12 chr11: 2,583,425-2,583,555	KCNQ1
nsv3877537	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 2,527,908-2,528,038 , GRCh37 chr11: 2,549,138-2,549,268	KCNQ1
nsv3872403	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 2,583,435-2,583,545 , GRCh37 chr11: 2,604,665-2,604,775	KCNQ1
nsv7093767	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,799,186-2,799,287 , GRCh38.p12 chr11: 2,777,956-2,778,057 , GRCh38.p12 chr11\|NT_187585.1: 10,143-10,244	KCNQ1
nsv3885662	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 2,591,838-2,594,236 , GRCh38 chr11: 2,570,608-2,573,006	KCNQ1
nsv6634658	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 2,606,440-2,606,441 , GRCh38 chr11: 2,585,210-2,585,211	KCNQ1
nsv4769351	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 2,604,775-2,608,798 , GRCh38 chr11: 2,583,545-2,587,568	KCNQ1
nsv4450530	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 2,608,790-2,608,932 , GRCh38 chr11: 2,587,560-2,587,702	KCNQ1

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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 78

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Number of Variants: 20

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Supplemental Content

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