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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685160	GRCh37/hg19 5q14.2(chr5:82300022-82443506)x1	SCARNA18, TMEM167A +1 more	Copy number loss	not provided	GUncertain significance
Select item 980159	GRCh37/hg19 5q14.2(chr5:82436326-82492676)x1	XRCC4	Copy number loss	not provided	GUncertain significance
Select item 814707	GRCh37/hg19 5q14.2(chr5:82511482-82566192)x1	XRCC4	Copy number loss	not provided	GUncertain significance
Select item 814706	GRCh37/hg19 5q14.2(chr5:82381505-82481677)x1	XRCC4	Copy number loss	not provided	GUncertain significance
Select item 814693	GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3	ACOT12, ADGRV1 +98 more	Copy number gain	not provided	GPathogenic
Select item 563084	GRCh37/hg19 5q14.2(chr5:82355242-82603880)x1	TMEM167A, XRCC4 +1 more	Copy number loss	not provided	GUncertain significance

ClinVar