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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809150	GRCh37/hg19 12q12(chr12:44655649-44831529)x1	TMEM117	Copy number loss	not provided	GUncertain significance
Select item 1808488	GRCh37/hg19 12q12(chr12:44080990-44354797)x1	IRAK4, PUS7L +2 more	Copy number loss	not provided	GUncertain significance
Select item 1807749	GRCh37/hg19 12q12(chr12:44290545-44457702)x1	TMEM117	Copy number loss	not provided	GUncertain significance
Select item 979962	GRCh37/hg19 12q12(chr12:43953566-46197331)x3	DBX2, ANO6 +6 more	Copy number gain	not provided	GUncertain significance
Select item 815523	GRCh37/hg19 12q12(chr12:44443029-44585529)x1	TMEM117	Copy number loss	not provided	GUncertain significance
Select item 563924	GRCh37/hg19 12q12(chr12:44091295-44354797)x1	PUS7L, TWF1 +2 more	Copy number loss	not provided	GUncertain significance
Select item 563921	GRCh37/hg19 12q12(chr12:44090896-44343135)x1	PUS7L, TWF1 +2 more	Copy number loss	not provided	GLikely benign

ClinVar