dbVar for Gene (Select 7490) - 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
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
nsv7093686	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 32,410,604-32,410,745 , GRCh38.p12 chr11: 32,389,058-32,389,199	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
nsv6904513	copy number variation	1	nstd229	human		GRCh38 chr11: 32,415,847-32,419,432 , GRCh37.p13 chr11: 32,437,393-32,440,978	WT1
nsv6902445	copy number variation	1	nstd229	human		GRCh38 chr11: 32,383,639-32,386,384 , GRCh37.p13 chr11: 32,405,185-32,407,930	WT1
nsv6900408	copy number variation	1	nstd229	human		GRCh38 chr11: 32,428,874-32,431,555 , GRCh37.p13 chr11: 32,450,420-32,453,101	WT1
nsv6898893	copy number variation	1	nstd229	human		GRCh38 chr11: 32,405,993-32,412,187 , GRCh37.p13 chr11: 32,427,539-32,433,733	WT1
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
nsv6465414	copy number variation	1	nstd223	human		GRCh38 chr11: 32,416,625-32,417,071 , GRCh37.p13 chr11: 32,438,171-32,438,617	WT1
nsv6458355	copy number variation	1	nstd223	human		GRCh38 chr11: 32,403,133-32,406,421 , GRCh37.p13 chr11: 32,424,679-32,427,967	WT1
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
nsv6247944	mobile element insertion	1	nstd215	human		GRCh38 chr11: 32,412,732-32,412,732 , GRCh37.p13 chr11: 32,434,278-32,434,278	WT1
nsv6081466	insertion	1	nstd212	human		GRCh38 chr11: 32,412,717-32,412,717 , GRCh37.p13 chr11: 32,434,263-32,434,263	WT1
nsv6081051	insertion	1	nstd212	human		GRCh38 chr11: 32,403,342-32,403,342 , GRCh37.p13 chr11: 32,424,888-32,424,888	WT1
nsv5968463	insertion	1	nstd209	human		GRCh38 chr11: 32,412,717-32,412,717 , GRCh37.p13 chr11: 32,434,263-32,434,263	WT1
nsv5702312	mobile element insertion	2	nstd211	human		GRCh38 chr11: 32,412,732-32,412,732 , GRCh37.p13 chr11: 32,434,278-32,434,278	WT1
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
nsv5672552	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,421,484-32,421,600 , GRCh38.p12 chr11: 32,399,938-32,400,054	WT1
nsv5653264	insertion	1	nstd207	human		GRCh38 chr11: 32,412,720-32,412,720 , GRCh37.p13 chr11: 32,434,266-32,434,266	WT1

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Number of Variants: 20

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Result Filters

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Organism

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 224

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Number of Variants: 20

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