"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TMEM65"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1175787	NM_194291.3(TMEM65):c.622-5_622-4del	TMEM65	Deletion (intron variant)	not provided	GLikely benign
Select item 2658795	NM_194291.3(TMEM65):c.144G>A (p.Pro48=)	LOC130001070, TMEM65	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024645	GRCh37/hg19 8q23.3-24.3(chr8:113392581-146364022)x3	LY6E, LY6H +173 more	Copy number gain	not provided	GPathogenic

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