"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PITX1"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2498978	NM_002653.5(PITX1):c.738del (p.Asn246fs)	PITX1 (N246fs)	Deletion (frameshift variant)	not provided	GLikely pathogenic
Select item 624508	GRCh37/hg19 5q23.2-31.2(chr5:126377719-136270989)x1	ACSL6, ADAMTS19 +68 more	Copy number loss	not provided	GLikely pathogenic
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign

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