kcna5[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4578652	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 5,153,314-5,155,155 , GRCh38.p12 chr12: 5,044,148-5,045,989	KCNA5
nsv7094144	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr12: 5,020,545-5,155,155 , GRCh38.p12 chr12: 4,911,379-5,045,989	KCNA5, KCNA1, 2 more genes
nsv4457052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, OTUD4P1, 59 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, 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	KCNA5, LOC105369677, 684 more genes

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

Send to:

Search results

Items: 1 to 20 of 62

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 62

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity