dbVar for Gene (Select 23332) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7098868	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 121,981,917-122,363,471 , GRCh38.p12 chr2: 121,224,341-121,605,895	CLASP1, TFCP2L1, 3 more genes
nsv7096196	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 121,684,917-122,288,605 , GRCh38.p12 chr2: 120,927,341-121,531,029	GLI2, RPS17P7, 6 more genes
nsv7056112	inversion	1	nstd229	human		GRCh38 chr2: 121,370,708-121,373,841 , GRCh37.p13 chr2: 122,128,284-122,131,417	CLASP1
nsv7054517	inversion	1	nstd229	human		GRCh38 chr2: 121,393,255-121,393,295 , GRCh37.p13 chr2: 122,150,831-122,150,871	CLASP1
nsv7052712	inversion	1	nstd229	human		GRCh38 chr2: 121,341,755-121,341,872 , GRCh37.p13 chr2: 122,099,331-122,099,448	CLASP1
nsv7050777	inversion	1	nstd229	human		GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831	LOC105373578, RPL17P15, 65 more genes
nsv6698010	copy number variation	1	nstd229	human		GRCh38 chr2: 121,614,223-121,624,703 , GRCh37.p13 chr2: 122,371,799-122,382,279	CLASP1
nsv6697034	copy number variation	1	nstd229	human		GRCh38 chr2: 121,605,387-121,605,528 , GRCh37.p13 chr2: 122,362,963-122,363,104	CLASP1
nsv6696801	copy number variation	1	nstd229	human		GRCh38 chr2: 120,749,236-121,378,541 , GRCh37.p13 chr2: 121,506,812-122,136,117	LOC105373587, RPS17P7, 4 more genes
nsv6696420	copy number variation	1	nstd229	human		GRCh38 chr2: 121,557,394-121,558,047 , GRCh37.p13 chr2: 122,314,970-122,315,623	CLASP1
nsv6696301	copy number variation	1	nstd229	human		GRCh38 chr2: 121,600,115-121,600,349 , GRCh37.p13 chr2: 122,357,691-122,357,925	CLASP1
nsv6696299	copy number variation	1	nstd229	human		GRCh38 chr2: 121,399,999-121,400,137 , GRCh37.p13 chr2: 122,157,575-122,157,713	CLASP1
nsv6695054	copy number variation	1	nstd229	human		GRCh38 chr2: 121,472,253-121,481,822 , GRCh37.p13 chr2: 122,229,829-122,239,398	CLASP1
nsv6695022	copy number variation	1	nstd229	human		GRCh38 chr2: 121,621,230-121,626,112 , GRCh37.p13 chr2: 122,378,806-122,383,688	CLASP1
nsv6694842	copy number variation	1	nstd229	human		GRCh38 chr2: 121,334,598-121,336,128 , GRCh37.p13 chr2: 122,092,174-122,093,704	CLASP1
nsv6694542	copy number variation	1	nstd229	human		GRCh38 chr2: 121,503,082-121,503,446 , GRCh37.p13 chr2: 122,260,658-122,261,022	CLASP1
nsv6694237	copy number variation	1	nstd229	human		GRCh38 chr2: 121,325,422-121,336,168 , GRCh37.p13 chr2: 122,082,998-122,093,744	CLASP1
nsv6692050	copy number variation	1	nstd229	human		GRCh38 chr2: 121,452,668-121,789,769 , GRCh37.p13 chr2: 122,210,244-122,547,345	RPL12P15, CLASP1-AS1, 8 more genes
nsv6691729	copy number variation	1	nstd229	human		GRCh38 chr2: 121,342,824-121,345,051 , GRCh37.p13 chr2: 122,100,400-122,102,627	CLASP1
nsv6691716	copy number variation	1	nstd229	human		GRCh38 chr2: 121,644,401-121,721,400 , GRCh37.p13 chr2: 122,401,977-122,478,976	NIFK-AS1, RPL12P15, 2 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:

Links from Gene

Items: 1 to 20 of 849

Number of Variants: 20

Send to:

Supplemental Content

Find related data

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

Links from Gene

Items: 1 to 20 of 849

Page of 43

Number of Variants: 20

Page of 43

Supplemental Content

Find related data

Recent activity