C3180937[trait identifier] AND "Daryl Scott Lab, Baylor College of Med - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2499630	GRCh38/hg38 15q11.2(chr15:22781888-23030923)	CYFIP1, LOC112272575 +14 more	Copy number loss	Chromosome 15q11.2 deletion syndrome	GUncertain significance
Select item 2499631	GRCh38/hg38 15q11.2(chr15:22787668-23051531)	CYFIP1, LOC112272575 +11 more	Copy number loss	Chromosome 15q11.2 deletion syndrome	GUncertain significance
Select item 2499632	GRCh38/hg38 15q11.2(chr15:22787849-23051049)	CYFIP1, LOC112272575 +10 more	Copy number loss	Chromosome 15q11.2 deletion syndrome	GUncertain significance

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ClinVar