"ISCA Site 6"[submitter] AND "BCHE"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 395532	GRCh37/hg19 3q26.1(chr3:163657369-167073454)x1	BCHE, SI +2 more	Copy number loss	See cases	GUncertain significance
Select item 394463	GRCh37/hg19 3q26.1(chr3:165491171-165547461)x1	BCHE	Copy number loss	See cases	GLikely benign
Select item 393885	GRCh37/hg19 3q25.32-29(chr3:158980631-197766890)x3	LRRC31, MCCC1 +198 more	Copy number gain	See cases	GPathogenic

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