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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685879	GRCh37/hg19 2q36.2-37.3(chr2:225995545-237594511)x3	ACKR3, AGAP1 +79 more	Copy number gain	not provided	GPathogenic
Select item 2685875	GRCh37/hg19 2q35-37.3(chr2:218376403-242783384)x3	AAMP, ABCB6 +208 more	Copy number gain	not provided	GPathogenic
Select item 980012	GRCh37/hg19 2q36.2-36.3(chr2:226027074-229110812)x1	SPHKAP, MFF +11 more	Copy number loss	not provided	GLikely pathogenic
Select item 816575	GRCh37/hg19 2q36.3(chr2:227766370-227857616)x1	RHBDD1	Copy number loss	not provided	GUncertain significance
Select item 814370	GRCh37/hg19 2q36.3(chr2:227763096-227818239)x1	RHBDD1	Copy number loss	not provided	GUncertain significance
Select item 562681	GRCh37/hg19 2q35-37.3(chr2:219225872-242016876)x3	ABCB6, ACKR3 +183 more	Copy number gain	not provided	GPathogenic
Select item 562506	GRCh37/hg19 2q36.3(chr2:227766478-227855256)x1	RHBDD1	Copy number loss	not provided	GUncertain significance

ClinVar