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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 8633	NM_000163.5(GHR):c.181C>T (p.Arg61Ter)	GHR (R61* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1808669	GRCh37/hg19 5p13.3-11(chr5:29348753-46389339)x3	ADAMTS12, AGXT2 +71 more	Copy number gain	not provided	GPathogenic
Select item 814684	GRCh37/hg19 5p13.1-q11.1(chr5:38432180-49441945)x3	GHR, CARD6 +31 more	Copy number gain	not provided	GPathogenic
Select item 563061	GRCh37/hg19 5p13.1-12(chr5:42488411-42705764)x3	GHR	Copy number gain	not provided	GUncertain significance
Select item 563060	GRCh37/hg19 5p13.1-12(chr5:41879642-42911463)x1	SELENOP, RIMOC1 +3 more	Copy number loss	not provided	GUncertain significance
Select item 563053	GRCh37/hg19 5p14.1-12(chr5:27227243-45685844)x3	C1QTNF3, C5orf22 +71 more	Copy number gain	not provided	GPathogenic

ClinVar