alg12[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
nsv7095842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 50,297,486-50,307,413 , GRCh38.p12 chr22: 49,903,838-49,913,765	ALG12
nsv7093155	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr22: 50,304,063-50,304,112 , GRCh38 chr22: 49,910,415-49,910,464	ALG12
nsv4454137	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr22: 49,903,818-49,907,964 , GRCh37 chr22: 50,297,466-50,301,612	ALG12
nsv6311275	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 50,297,486-50,301,612 , GRCh38.p12 chr22: 49,903,838-49,907,964	ALG12
nsv3908197	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,282,986-50,301,664 , GRCh38.p12 chr22: 49,889,338-49,908,016	ALG12, ZBED4
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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, 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	ALG12, LINC01656, 156 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 146

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 146

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Search details

Recent activity