dbVar for Gene (Select 51352) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7094167	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,410,604-32,460,464 , GRCh38.p12 chr11: 32,389,058-32,438,918	WT1-AS, WT1
nsv7093682	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 30,253,450-32,460,464 , GRCh38.p12 chr11: 30,231,903-32,438,918	ARL14EP, PAX6, 28 more genes
nsv6902675	copy number variation	1	nstd229	human		GRCh38 chr11: 32,455,312-32,459,156 , GRCh37.p13 chr11: 32,476,858-32,480,702	WT1-AS
nsv6902467	copy number variation	1	nstd229	human		GRCh38 chr11: 32,450,735-32,450,784 , GRCh37.p13 chr11: 32,472,281-32,472,330	WT1-AS
nsv6898882	copy number variation	1	nstd229	human		GRCh38 chr11: 32,447,923-32,451,715 , GRCh37.p13 chr11: 32,469,469-32,473,261	WT1-AS
nsv6638023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766	THEM7P, LOC105376624, 92 more genes
nsv6634446	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 32,416,364-32,579,393 , GRCh38.p12 chr11: 32,394,818-32,557,847	WT1, WT1-AS
nsv6309193	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 31,669,269-32,460,464 , GRCh38.p12 chr11: 31,647,721-32,438,918	LOC107984322, PAX6-AS1, 13 more genes
nsv5968049	insertion	1	nstd209	human		GRCh38 chr11: 32,440,072-32,440,072 , GRCh37.p13 chr11: 32,461,618-32,461,618	WT1-AS
nsv5729275	mobile element insertion	1	nstd211	human		GRCh38 chr11: 32,456,682-32,456,682 , GRCh37.p13 chr11: 32,478,228-32,478,228	WT1-AS
nsv5672553	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,456,236-32,460,464 , GRCh38.p12 chr11: 32,434,690-32,438,918	WT1, WT1-AS
nsv5495615	copy number variation	1	nstd206	human		GRCh38 chr11: 32,451,030-32,458,081 , GRCh37.p13 chr11: 32,472,576-32,479,627	WT1-AS
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv4986956	copy number variation	1	nstd200	human		GRCh38 chr11: 32,451,090-32,458,081 , GRCh37.p13 chr11: 32,472,636-32,479,627	WT1-AS
nsv4838502	copy number variation	1	nstd200	human		GRCh37 chr11: 32,472,636-32,479,627 , GRCh38.p12 chr11: 32,451,090-32,458,081	WT1-AS
nsv4751865	inversion	1	nstd199	human		GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187	, ACP2, 1686 more genes
nsv4741272	copy number variation	1	nstd199	human		GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605	, DRAP1, 1535 more genes
nsv4683317	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,456,236-32,456,891 , GRCh38.p12 chr11: 32,434,690-32,435,345	WT1-AS, WT1
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	BGLT3, RPL21P97, 723 more genes
nsv4674824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344	SNORA88, LINC02729, 305 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 150

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 150

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Recent activity