pan2[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
nsv4457488	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 56,309,732-56,393,350 , GRCh38.p12 chr19: 55,798,366-55,881,984	NLRP4, NLRP11
nsv3890137	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 56,376,574-56,477,587 , GRCh38.p12 chr19: 55,865,208-55,966,221	NLRP13, NLRP4, 1 more genes
nsv3903978	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 56,286,299-56,368,427 , GRCh38.p12 chr19: 55,774,933-55,857,061	NLRP4, RFPL4AP1, 1 more genes
nsv6638017	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 56,286,281-56,395,259 , GRCh38.p12 chr19: 55,774,915-55,883,893	NLRP4, RFPL4AP1, 1 more genes
nsv4729938	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 56,273,044-56,374,621 , GRCh38.p12 chr19: 55,761,678-55,863,255	NLRP4, NLRP11, 3 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CYP1B1-AS1, LOC107985771, 1649 more genes
nsv4451022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621	RAD51AP2, LOC101928149, 82 more genes
nsv3891917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 16,904,863-21,823,606 , GRCh38 chr2: 16,723,596-21,600,734 , NCBI36 chr2: 16,768,344-21,677,111	LOC105373454, RAD51AP2, 68 more genes
nsv6112733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735	LOC112267888, LOC105373454, 40 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	LOC112268439, RNA5SP116, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IGKV2OR2-10, LOC105374848, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	RNU6-674P, KANSL3, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	MTND2P22, LOC112268410, 3724 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	PAN2, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	PAN2, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	PAN2, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	PAN2, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	PAN2, OR5BT1P, 2441 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ZNF321P, ZNF861P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	BABAM1, BEST2, 2426 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 69

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 69

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity