cdh23[All Fields] AND 1[has_clinical] - 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
nsv7093646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,439,124-73,447,496 , GRCh38.p12 chr10: 71,679,367-71,687,739	CDH23
nsv6309007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,437,203-73,439,259 , GRCh38.p12 chr10: 71,677,446-71,679,502	CDH23
nsv7093892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,537,936-73,539,214 , GRCh38.p12 chr10: 71,778,179-71,779,457	CDH23
nsv7093890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,466,676-73,467,843 , GRCh38.p12 chr10: 71,706,919-71,708,086	CDH23
nsv7093889	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,464,658-73,464,897 , GRCh38.p12 chr10: 71,704,901-71,705,140	CDH23
nsv5672531	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,442,182-73,442,349 , GRCh38.p12 chr10: 71,682,425-71,682,592	CDH23
nsv6309077	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,375,251-73,375,383 , GRCh38.p12 chr10: 71,615,494-71,615,626	CDH23
nsv4681376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,442,202-73,442,329 , GRCh38.p12 chr10: 71,682,445-71,682,572	CDH23
nsv6309160	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,447,394-73,447,486 , GRCh38.p12 chr10: 71,687,637-71,687,729	CDH23
nsv4682285	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,199,589-73,199,655 , GRCh38.p12 chr10: 71,439,832-71,439,898	CDH23
nsv4682477	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr10: 73,337,661-73,337,759 , GRCh38.p12 chr10: 71,577,904-71,578,002	CDH23
nsv6314675	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 73,454,017-73,468,962 , GRCh38.p12 chr10: 71,694,260-71,709,205	CDH23
nsv4685597	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 73,405,588-73,406,374 , GRCh38.p12 chr10: 71,645,831-71,646,617	CDH23
nsv6308923	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 73,206,055-73,206,172 , GRCh38.p12 chr10: 71,446,298-71,446,415	CDH23
nsv3906054	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 73,129,458-73,162,237 , GRCh38.p12 chr10: 71,369,701-71,402,480	CDH23
nsv3903073	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 73,141,020-73,157,945 , GRCh38.p12 chr10: 71,381,263-71,398,188	CDH23
nsv3900747	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 73,154,073-73,157,945 , GRCh38.p12 chr10: 71,394,316-71,398,188	CDH23
nsv4683064	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,403,618-73,407,489 , GRCh38.p12 chr10: 71,643,861-71,647,732	CDH23
nsv6309159	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 73,403,598-73,406,394 , GRCh38.p12 chr10: 71,643,841-71,646,637	CDH23
nsv6290825	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 73,405,588-73,406,374 , GRCh38.p12 chr10: 71,645,831-71,646,617	CDH23

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Number of Variants: 20

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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 57

Page of 3

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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