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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685487	GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1	HIF1A, HIF1A-AS2 +47 more	Copy number loss	not provided	GPathogenic
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 1808424	GRCh37/hg19 14q22.3(chr14:56811156-57163828)x3	TMEM260	Copy number gain	not provided	GUncertain significance
Select item 1339973	GRCh37/hg19 14q22.3(chr14:56816534-57163828)x3	TMEM260	Copy number gain	not provided	GUncertain significance
Select item 980491	GRCh37/hg19 14q22.3(chr14:56916550-57111448)x1	TMEM260	Copy number loss	not provided	GUncertain significance
Select item 815660	GRCh37/hg19 14q22.3-23.1(chr14:56605398-59404256)x1	ACTR10, AP5M1 +14 more	Copy number loss	not provided	GPathogenic
Select item 815659	GRCh37/hg19 14q22.3(chr14:55615073-58043694)x1	ATG14, FBXO34 +11 more	Copy number loss	not provided	GPathogenic
Select item 564085	GRCh37/hg19 14q22.3(chr14:57069274-57097693)x1	TMEM260	Copy number loss	not provided	GUncertain significance

ClinVar