kif26a[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
nsv3896479	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 104,639,442-104,646,326 , GRCh38.p12 chr14: 104,173,105-104,179,989	KIF26A
nsv3897222	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 104,638,180-104,645,048 , GRCh38.p12 chr14: 104,171,843-104,178,711	KIF26A
nsv3907458	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 104,639,439-104,646,027 , GRCh38.p12 chr14: 104,173,102-104,179,690	KIF26A
nsv3906537	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 104,639,439-104,645,048 , GRCh38.p12 chr14: 104,173,102-104,178,711	KIF26A
nsv3896744	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 104,641,730-104,645,048 , GRCh38.p12 chr14: 104,175,393-104,178,711	KIF26A
nsv3914561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 95,990,744-107,287,708 , GRCh38 chr14: 95,524,407-106,879,501 , NCBI36 chr14: 95,060,497-106,358,753	KIF26A, MIR889, 517 more genes
nsv4684265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456	KIF26A, NDUFB3P4, 502 more genes
nsv3911746	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 97,938,637-106,855,263 , GRCh37 chr14: 98,404,974-107,263,478 , NCBI36 chr14: 97,474,727-106,334,523	KIF26A, MIR1185-2, 477 more genes
nsv3921506	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523	KIF26A, RPL21P13, 453 more genes
nsv3902723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,661,319-107,285,437 , GRCh38.p12 chr14: 100,194,982-106,877,229	KIF26A, NDUFB3P4, 448 more genes
nsv3922827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523	KIF26A, RNU6-1316P, 440 more genes
nsv3914191	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 100,118,149-106,356,482 , GRCh38 chr14: 100,582,059-106,877,229 , GRCh37 chr14: 101,048,396-107,285,437	KIF26A, IGHV4-55, 436 more genes
nsv3918080	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 100,344,390-106,334,523 , GRCh37 chr14: 101,274,637-107,263,478 , GRCh38 chr14: 100,808,300-106,855,263	KIF26A, GPR132, 427 more genes
nsv6314048	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229	KIF26A, IGHD4-23, 329 more genes
nsv4456944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681	KIF26A, IGHV1-58, 308 more genes
nsv3917997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,131,939-107,263,478 , NCBI36 chr14: 101,201,692-106,334,523 , GRCh38 chr14: 101,665,602-106,855,263	KIF26A, IGHV3-23, 315 more genes
nsv3917679	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 101,925,670-106,876,323 , GRCh37 chr14: 102,392,007-107,284,531 , NCBI36 chr14: 101,461,760-106,355,576	KIF26A, LINC00221, 313 more genes
nsv4729218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229	KIF26A, IGHV4-61, 308 more genes
nsv3893817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,670,706-107,285,437 , GRCh38.p12 chr14: 102,204,369-106,877,229	KIF26A, MOK, 308 more genes
nsv3914922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 102,239,422-106,877,229 , GRCh37 chr14: 102,705,759-107,285,437 , NCBI36 chr14: 101,775,512-106,356,482	KIF26A, GPR132, 306 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 64

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 64

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity