C4021789[trait identifier] AND "Clinical Genetics Research Group, Karo - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638674	GRCh37/hg19 7q34(chr7:139478979-139550968)	TBXAS1	Copy number gain	Imperforate anus +4 more	GUncertain significance
Select item 638675	GRCh37/hg19 15q12(chr15:27462869-27544157)	GABRG3	Copy number gain	Imperforate anus +4 more	GUncertain significance
Select item 638672	GRCh37/hg19 22q11.22-11.23(chr22:22971867-23643138)	IGLC1, BCR +5 more	Copy number loss	Ventricular septal defect +2 more	GPathogenic

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