epha4[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
nsv5200285	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 222,199,886-222,298,997 , GRCh38.p12 chr2: 221,335,166-221,434,277	EPHA4
nsv3883789	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 221,819,192-222,401,086 , GRCh38.p12 chr2: 220,954,472-221,536,366	EPHA4, TMEM256P2
nsv7096243	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 222,290,748-222,436,968 , GRCh38.p12 chr2: 221,426,028-221,572,248	EPHA4, TMEM256P2
nsv6290271	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 222,290,748-222,436,968 , GRCh38.p12 chr2: 221,426,028-221,572,248	EPHA4, TMEM256P2
nsv3903833	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 221,410,796-222,200,580 , GRCh37 chr2: 221,702,552-222,492,336 , GRCh38 chr2: 220,837,832-221,627,616	EPHA4, RPL23P5, 3 more genes
nsv3893296	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr2: 221,960,583-222,172,307 , GRCh37 chr2: 222,252,339-222,464,063 , GRCh38 chr2: 221,387,619-221,599,343	EPHA4, LOC105373897, 2 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	EPHA4, DAZAP2P1, 2991 more genes
nsv6313668	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062	EPHA4, LOC105373947, 357 more genes
nsv3873368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 218,813,434-227,450,699 , GRCh38.p12 chr2: 217,948,711-226,585,983	EPHA4, ARPC2, 163 more genes
nsv6112757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 220,056,891-227,164,817 , GRCh38.p12 chr2: 219,192,169-226,300,101	EPHA4, DES, 100 more genes
nsv3906433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 219,946,342-226,295,024 , GRCh38 chr2: 219,081,620-225,430,308 , NCBI36 chr2: 219,654,586-226,003,268	EPHA4, HIGD1AP4, 102 more genes
nsv3873167	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 220,614,743-225,587,770 , GRCh38.p12 chr2: 219,750,021-224,723,053	EPHA4, SCG2, 59 more genes
nsv3888475	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 221,439,250-226,170,404 , GRCh38.p12 chr2: 220,574,529-225,305,687	EPHA4, FAM124B, 55 more genes
nsv3879172	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 220,608,798-224,217,756 , GRCh38.p12 chr2: 219,744,076-223,353,038	EPHA4, LOC100419511, 43 more genes
nsv3877541	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 222,150,306-223,174,130 , GRCh38.p12 chr2: 221,285,586-222,309,411	EPHA4, LOC105373899, 11 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	EPHA4, 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	EPHA4, 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	EPHA4, 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	EPHA4, MTND2P22, 3724 more genes
nsv4728725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306	EPHA4, LOC105376755, 1013 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 38

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 38

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity