C0036572[trait identifier] AND "Medical Genetics Lab, Policlinico S. O - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559502	GRCh37/hg19 2p23.3(chr2:24807000-25700000)x3	CENPO, PTRHD1 +7 more	Copy number gain	Fetal growth restriction +4 more	GUncertain significance
Select item 559399	Single allele	C9orf163, DIPK1B +5 more	Duplication	Seizure +4 more	GUncertain significance
Select item 559401	Single allele	AMBRA1, CHRM4 +4 more	Duplication	Global developmental delay +4 more	GUncertain significance
Select item 559404	Single allele	GDPD2, DLG3 +5 more	Duplication	Seizure	GLikely pathogenic

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