"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "EPHB6"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2658106	NM_004445.6(EPHB6):c.1988C>T (p.Ala663Val)	EPHB6 (A370V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2270793	NM_004445.6(EPHB6):c.2714G>A (p.Arg905Gln)	EPHB6 (R612Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GLikely benign
Select item 2583057	GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1	C7orf33, CASP2 +125 more	Copy number loss	not provided	GPathogenic

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