tspo[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, 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	TSPO, LOC101927474, 165 more genes
nsv6313968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,451,316-46,662,660 , GRCh38.p12 chr22: 43,055,310-46,266,763	TSPO, EFCAB6-DT, 82 more genes
nsv5673276	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994	TSPO, RPL5P34, 48 more genes
nsv5381088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996	TSPO, CYP2D8P, 49 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:

Search results

Items: 1 to 20 of 51

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 51

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity