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

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685464	GRCh37/hg19 13q14.11(chr13:44141531-44296623)x1	ENOX1	Copy number loss	not provided	GUncertain significance
Select item 1807946	GRCh37/hg19 13q14.11(chr13:43935405-44158625)x1	ENOX1	Copy number loss	not provided	GUncertain significance
Select item 1341277	GRCh37/hg19 13q14.11-33.3(chr13:42504540-108206269)x3	GTF2F2, PRR20D +175 more	Copy number gain	not provided	GPathogenic
Select item 1341081	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 1340462	GRCh37/hg19 13q14.11-14.12(chr13:43688967-45630698)x1	CCDC122, ENOX1 +6 more	Copy number loss	not provided	GUncertain significance
Select item 815585	GRCh37/hg19 13q14.11(chr13:44010123-44252546)x1	ENOX1	Copy number loss	not provided	GUncertain significance
Select item 815584	GRCh37/hg19 13q14.11(chr13:43163675-43887005)x3	TNFSF11, EPSTI1 +3 more	Copy number gain	not provided	GUncertain significance
Select item 564083	GRCh37/hg19 13q11-22.1(chr13:19436286-74045459)x3	NUDT15, NUFIP1 +211 more	Copy number gain	not provided	GPathogenic
Select item 564049	GRCh37/hg19 13q14.11(chr13:43159134-44041338)x4	TNFSF11, DNAJC15 +3 more	Copy number gain	not provided	GUncertain significance
Select item 564028	GRCh37/hg19 13q14.11(chr13:43688966-44021703)x1	ENOX1	Copy number loss	not provided	GUncertain significance