"The Division of Genetics and Genomic Medicine, Washington University - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619146	GRCh38/hg38 3p26.3(chr3:1716762-2204464)x3	CNTN4-AS2, LOC122889017 +1 more	Copy number gain	Delayed speech and language development	GUncertain significance
Select item 619147	GRCh38/hg38 3p26.3(chr3:2077327-2515335)x3	CNTN4, CNTN4-AS2 +3 more	Copy number gain	Delayed speech and language development	GUncertain significance
Select item 619145	GRCh38/hg38 3p26.2(chr3:2878363-3006381)x1	CNTN4, LOC129389017 +4 more	Copy number loss	Delayed speech and language development	GUncertain significance

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ClinVar