pfn4[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
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	PFN4, CYP1B1-AS1, 1649 more genes
nsv3890734	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,656,029-28,601,557 , GRCh37 chr2: 22,802,524-28,748,053 , GRCh38 chr2: 22,579,652-28,525,186	PFN4, MAPRE3-AS1, 142 more genes
nsv3873411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 19,905,995-24,762,790 , GRCh38.p12 chr2: 19,706,234-24,539,921	PFN4, LOC100130841, 77 more genes
nsv6314937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,439,520-25,608,211 , GRCh38.p12 chr2: 22,216,648-25,385,342	PFN4, ITSN2, 50 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	PFN4, LOC112268439, 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	PFN4, IGKV2OR2-10, 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	PFN4, RNU6-674P, 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	PFN4, MTND2P22, 3724 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	PFN4, SLC35F6, 801 more genes
nsv3908288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875	PFN4, ALLC, 674 more genes
nsv6636815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573	PFN4, LOC105374455, 504 more genes
nsv3908038	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509	PFN4, LOC105373394, 507 more genes
nsv3879320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230	PFN4, ATL2, 465 more genes
nsv3907033	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531	PFN4, GTF3C2-AS1, 434 more genes
nsv3893260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 17,019-26,541,714 , GRCh38 chr2: 17,019-26,318,846 , NCBI36 chr2: 7,019-26,395,218	PFN4, LOC102723389, 362 more genes
nsv3896997	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 12,770-25,039,694 , GRCh37 chr2: 12,770-25,262,563 , NCBI36 chr2: 2,770-25,116,067	PFN4, LOC105373359, 333 more genes
nsv3919769	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010	PFN4, RNA5SP88, 213 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	PFN4, LOC101927723, 1246 more genes
nsv3871929	copy number variation	1	nstd102	human	not provided	GRCh37 chr2: 24,235,780-25,700,427 , GRCh38.p12 chr2: 24,012,910-25,477,558	PFN4, HMGN2P20, 32 more genes
nsv3882368	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 24,315,204-26,384,655 , GRCh38.p12 chr2: 24,092,334-26,161,786	PFN4, TPM3P7, 41 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 21

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 21

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity