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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684714	GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3	ABHD12B, ABHD4 +289 more	Copy number gain	not provided	GPathogenic
Select item 1809348	GRCh37/hg19 14q12-13.1(chr14:24959823-33415359)x1	AKAP6, AP4S1 +19 more	Copy number loss	not provided	GPathogenic
Select item 1807987	GRCh37/hg19 14q13.1(chr14:33656354-34157207)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 1341281	GRCh37/hg19 14q13.1(chr14:33656353-34162087)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 1340713	GRCh37/hg19 14q13.1(chr14:33766967-34010728)x1	NPAS3	Copy number loss	not provided	GUncertain significance
Select item 980482	GRCh37/hg19 14q13.1(chr14:34190493-34678663)x1	NPAS3, EGLN3	Copy number loss	not provided	GUncertain significance
Select item 980481	GRCh37/hg19 14q13.1(chr14:33463166-33998038)x1	NPAS3	Copy number loss	not provided	GLikely benign
Select item 815628	GRCh37/hg19 14q11.2-21.2(chr14:20511672-44829030)x3	ABHD4, ACIN1 +187 more	Copy number gain	not provided	GPathogenic

ClinVar