pick1[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
nsv3910315	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 36,720,045-36,792,737 , GRCh38 chr22: 37,994,092-38,066,784 , GRCh37 chr22: 38,390,099-38,462,791	PICK1, POLR2F
nsv3922128	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177	PICK1, LOC102724378, 120 more genes
nsv7095836	copy number variation	3	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628	PICK1, CSF2RBP1, 80 more genes
nsv3904443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 36,877,226-38,548,989 , GRCh38.p12 chr22: 36,481,179-38,152,982	PICK1, LOC107985576, 63 more genes
nsv3915039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 37,447,222-39,103,680 , GRCh37 chr22: 37,843,259-39,499,685 , NCBI36 chr22: 36,173,205-37,829,631	PICK1, MIR4534, 68 more genes
nsv7096310	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,097,373-39,306,081 , GRCh38.p12 chr22: 37,701,366-38,910,076	PICK1, TMEM184B, 46 more genes
nsv3892449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 37,866,631-39,054,815 , GRCh38.p12 chr22: 37,470,593-38,658,810	PICK1, MIR658, 48 more genes
nsv3913000	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,117,784-39,282,669 , GRCh38 chr22: 37,721,777-38,886,664 , NCBI36 chr22: 36,447,730-37,612,615	PICK1, DDX17, 46 more genes
nsv4676116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065	PICK1, CSNK1E, 43 more genes
nsv5200376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 38,155,164-38,541,997 , GRCh38.p12 chr22: 37,759,157-38,145,990	PICK1, H1-0, 18 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	PICK1, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	PICK1, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	PICK1, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	PICK1, FBXO7, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	PICK1, FABP5P11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	PICK1, DDTL, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	PICK1, YPEL1, 1083 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	PICK1, IGLV3-27, 1082 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	PICK1, POM121L7P, 1082 more genes
nsv3913775	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264	PICK1, ZNF280A, 1059 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 30

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 30

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity