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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808968	GRCh37/hg19 12q21.2(chr12:76812664-76891516)x1	OSBPL8	Copy number loss	not provided	GUncertain significance
Select item 1340527	GRCh37/hg19 12q15-21.2(chr12:70084476-77065764)x1	TBC1D15, THAP2 +25 more	Copy number loss	not provided	GPathogenic
Select item 980444	GRCh37/hg19 12q21.2(chr12:76557730-76885572)x3	BBS10, OSBPL8	Copy number gain	not provided	GLikely benign
Select item 815537	GRCh37/hg19 12q21.2(chr12:76708985-76800739)x1	BBS10, OSBPL8	Copy number loss	not provided	GUncertain significance

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ClinVar