"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 2684953	GRCh37/hg19 2q34(chr2:212633377-213434225)x1	ERBB4	Copy number loss	not provided	GUncertain significance
Select item 1808152	GRCh37/hg19 2q34(chr2:213290522-214539066)x3	ERBB4, IKZF2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1807601	GRCh37/hg19 2q34(chr2:212597211-213804569)x3	ERBB4	Copy number gain	not provided	GUncertain significance
Select item 1340248	GRCh37/hg19 2q34(chr2:213359350-213473331)x1	ERBB4	Copy number loss	not provided	GLikely benign
Select item 979400	GRCh37/hg19 2q33.2-34(chr2:204445619-212580788)x1	ACADL, ADAM23 +36 more	Copy number loss	not provided	GPathogenic
Select item 816558	GRCh37/hg19 2q34(chr2:213107280-213328411)x1	ERBB4	Copy number loss	not provided	GUncertain significance
Select item 814362	GRCh37/hg19 2q34(chr2:212184096-212747758)x1	ERBB4	Copy number loss	not provided	GUncertain significance
Select item 562677	GRCh37/hg19 2q33.3-35(chr2:205169148-219149293)x3	AAMP, ABCA12 +60 more	Copy number gain	not provided	GPathogenic
Select item 562554	GRCh37/hg19 2q34(chr2:212818448-213065294)x1	ERBB4	Copy number loss	not provided	GUncertain significance
Select item 562547	GRCh37/hg19 2q34(chr2:212678164-212895911)x1	ERBB4	Copy number loss	not provided	GUncertain significance
Select item 562509	GRCh37/hg19 2q34(chr2:213092401-213187551)x1	ERBB4	Copy number loss	not provided	GUncertain significance