celsr1[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
nsv3902558	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr22: 46,802,610-47,050,585 , GRCh38.p12 chr22: 46,406,713-46,654,688	CELSR1, FAM136EP, 2 more genes
nsv3897314	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 46,831,965-47,009,871 , GRCh38.p12 chr22: 46,436,068-46,613,974	CELSR1, GRAMD4, 2 more genes
nsv3900214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300	CELSR1, TYMP, 218 more genes
nsv6290298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638	CELSR1, CERK, 212 more genes
nsv3912011	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264	CELSR1, TUBGCP6, 213 more genes
nsv5381149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300	CELSR1, WBP2NL, 210 more genes
nsv4351202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331	CELSR1, PLXNB2, 204 more genes
nsv3893572	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410	CELSR1, CYP2D8P, 206 more genes
nsv3920027	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 42,433,752-50,738,932 , NCBI36 chr22: 41,159,702-49,524,226 , GRCh37 chr22: 42,829,758-51,177,360	CELSR1, MIR6821, 187 more genes
nsv3909355	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,955,616-51,183,840 , GRCh38.p12 chr22: 42,559,610-50,745,412	CELSR1, LOC101927499, 182 more genes
nsv6314059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410	CELSR1, TRABD, 181 more genes
nsv3897841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,050,743-51,197,838 , GRCh38.p12 chr22: 42,654,737-50,759,410	CELSR1, LINC00229, 176 more genes
nsv3905339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,111,156-51,183,840 , GRCh38.p12 chr22: 42,715,150-50,745,412	CELSR1, RPL5P34, 174 more genes
nsv3911529	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 41,552,196-49,525,130 , GRCh37 chr22: 43,222,252-51,178,264 , GRCh38 chr22: 42,826,246-50,739,836	CELSR1, TAFA5, 169 more genes
nsv3912301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,233,100-51,174,234 , GRCh38 chr22: 42,837,094-50,735,806 , NCBI36 chr22: 41,563,044-49,521,100	CELSR1, TTLL8, 168 more genes
nsv3900468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,320,284-51,183,840 , GRCh38.p12 chr22: 42,924,278-50,745,412	CELSR1, CHKB, 166 more genes
nsv3923135	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 42,493,445-50,268,479 , GRCh37 chr22: 42,889,451-50,706,908 , NCBI36 chr22: 41,219,395-49,049,035	CELSR1, LINC01656, 156 more genes
nsv3902752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,381,459-51,197,838 , GRCh38.p12 chr22: 42,985,453-50,759,410	CELSR1, SCO2, 168 more genes
nsv4685945	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 43,032,129-50,739,836 , GRCh37.p13 chr22: 43,428,135-51,178,264	CELSR1, LOC101927474, 165 more genes
nsv3911699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,583,986-51,183,872 , NCBI36 chr22: 41,913,930-49,530,738 , GRCh38 chr22: 43,187,980-50,745,444	CELSR1, PNPLA3, 158 more genes

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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 97

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Number of Variants: 20

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Search details

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