Related gene-specific medical variations for Gene (Select 2044) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685971	GRCh37/hg19 4q13.1(chr4:65890760-66503982)x3	EPHA5	Copy number gain	not provided	GUncertain significance
Select item 2685113	GRCh37/hg19 4q13.1-13.2(chr4:65293814-67567104)x1	EPHA5	Copy number loss	not provided	GUncertain significance
Select item 1809299	GRCh37/hg19 4q13.1(chr4:65952175-66507443)x3	EPHA5	Copy number gain	not provided	GUncertain significance
Select item 1340401	GRCh37/hg19 4q13.1(chr4:65824021-66365406)x3	EPHA5	Copy number gain	not provided	GUncertain significance
Select item 980090	GRCh37/hg19 4q13.1-13.2(chr4:65650283-66813883)x1	EPHA5	Copy number loss	not provided	GUncertain significance
Select item 442568	GRCh37/hg19 4q13.1-13.2(chr4:65999842-67635149)x1	EPHA5	Copy number loss	See cases	GUncertain significance
Select item 376701	NM_001281766.3(EPHA5):c.1748G>A (p.Gly583Glu)	EPHA5 (G514E +2 more)	Single nucleotide variant (missense variant)	Lung adenocarcinoma	GLikely pathogenic

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