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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685981	GRCh37/hg19 4q22.1(chr4:91296256-93417077)x3	CCSER1, GRID2	Copy number gain	not provided	GUncertain significance
Select item 2685980	GRCh37/hg19 4q22.1-22.2(chr4:90821342-93994597)x3	CCSER1, GRID2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1808037	GRCh37/hg19 4q22.1(chr4:91196374-91322634)x1	CCSER1	Copy number loss	not provided	GUncertain significance
Select item 1341211	GRCh37/hg19 4q21.21-22.1(chr4:80467886-93362064)x1	ABCG2, ABRAXAS1 +58 more	Copy number loss	not provided	GPathogenic
Select item 1340525	GRCh37/hg19 4q22.1(chr4:90943592-91196145)x3	CCSER1	Copy number gain	not provided	GUncertain significance
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 980108	GRCh37/hg19 4q22.1(chr4:91580496-92874676)x3	CCSER1	Copy number gain	not provided	GUncertain significance
Select item 980107	GRCh37/hg19 4q22.1(chr4:91852768-93447869)x1	CCSER1, GRID2	Copy number loss	not provided	GUncertain significance
Select item 980104	GRCh37/hg19 4q22.1(chr4:92491756-93233588)x3	CCSER1, GRID2	Copy number gain	not provided	GLikely benign
Select item 562945	GRCh37/hg19 4q22.1-22.3(chr4:90005204-96971785)x1	CCSER1, UNC5C +11 more	Copy number loss	not provided	GPathogenic
Select item 562937	GRCh37/hg19 4q21.21-22.3(chr4:81314915-96636651)x1	ABCG2, ABRAXAS1 +60 more	Copy number loss	not provided	GPathogenic