"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685445	GRCh37/hg19 12q21.32(chr12:86854062-86919682)x1	MGAT4C	Copy number loss	not provided	GUncertain significance
Select item 980449	GRCh37/hg19 12q21.31-21.32(chr12:85812496-86797077)x3	NTS, MGAT4C +1 more	Copy number gain	not provided	GUncertain significance
Select item 980448	GRCh37/hg19 12q21.31-21.32(chr12:86017618-86786974)x3	RASSF9, MGAT4C +1 more	Copy number gain	not provided	GLikely benign
Select item 980447	GRCh37/hg19 12q21.31(chr12:86432529-86529656)x1	MGAT4C	Copy number loss	not provided	GUncertain significance
Select item 815543	GRCh37/hg19 12q21.32(chr12:87121778-87551060)x1	MGAT4C	Copy number loss	not provided	GUncertain significance
Select item 815542	GRCh37/hg19 12q21.31(chr12:86173243-86421728)x3	RASSF9, NTS +1 more	Copy number gain	not provided	GUncertain significance
Select item 563978	GRCh37/hg19 12q21.31-21.32(chr12:86115942-88186381)x1	MGAT4C, NTS +1 more	Copy number loss	not provided	GUncertain significance
Select item 563967	GRCh37/hg19 12q21.32(chr12:86804191-87905416)x3	MGAT4C	Copy number gain	not provided	GUncertain significance
Select item 563941	GRCh37/hg19 12q21.32(chr12:87188645-87582711)x1	MGAT4C	Copy number loss	not provided	GLikely benign

ClinVar