kcna6[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
nsv3900863	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 4,930,100-4,954,591 , GRCh38.p12 chr12: 4,820,934-4,845,425	KCNA6
nsv4457052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926	KCNA6, TSPAN9, 118 more genes
nsv3906935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,201,932 , GRCh38.p12 chr12: 64,620-6,092,766	KCNA6, LRTM2, 113 more genes
nsv3907924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,039,841 , GRCh38.p12 chr12: 64,620-5,930,675	KCNA6, SLC6A13, 111 more genes
nsv3901202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-5,952,112 , GRCh38.p12 chr12: 64,620-5,842,946	KCNA6, LOC105369595, 110 more genes
nsv3910984	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 179,323-5,786,793 , GRCh37 chr12: 309,062-5,916,532 , GRCh38 chr12: 199,896-5,807,366	KCNA6, LOC107987182, 106 more genes
nsv6313933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 2,790,077-5,325,700 , GRCh38.p12 chr12: 2,680,911-5,216,534	KCNA6, OTUD4P1, 59 more genes
nsv3920162	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 2,472,155-4,809,269 , GRCh37 chr12: 2,601,894-4,939,008 , GRCh38 chr12: 2,492,728-4,829,842	KCNA6, RPL23AP14, 55 more genes
nsv5381764	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 3,619,010-5,221,363 , GRCh38.p12 chr12: 3,509,844-5,112,197	KCNA6, OTUD4P1, 30 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	KCNA6, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	KCNA6, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	KCNA6, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	KCNA6, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	KCNA6, OR5BT1P, 2441 more genes
nsv3914427	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 18,636-36,150,744 , GRCh37.p13 chr12: 148,375-37,864,477 , GRCh38.p12 chr12: 43,334-37,470,675	KCNA6, LOC105369667, 684 more genes
nsv3905633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499	KCNA6, RESF1, 684 more genes
nsv3897151	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305	KCNA6, CACNA2D4, 684 more genes
nsv4674941	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499	KCNA6, LOC105376675, 682 more genes
nsv3924262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104	KCNA6, ENO2, 684 more genes
nsv3901714	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-34,835,837 , GRCh38.p12 chr12: 64,620-34,682,902	KCNA6, LOC105369677, 684 more genes

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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 61

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Number of Variants: 20

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