"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "HSP90AA - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 720694	NM_005348.4(HSP90AA1):c.2089+7C>A	HSP90AA1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 782308	NM_005348.4(HSP90AA1):c.2079A>G (p.Lys693=)	HSP90AA1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 785469	NM_005348.4(HSP90AA1):c.1338+9A>G	HSP90AA1, LOC126862061	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 720695	NM_005348.4(HSP90AA1):c.1284G>A (p.Ala428=)	HSP90AA1, LOC126862061	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3244018	NC_000014.8:g.(?_102431029)_(103397017_?)dup	AMN, ANKRD9 +9 more	Duplication	Charcot-Marie-Tooth disease axonal type 2O	GUncertain significance
Select item 2424156	NC_000014.8:g.(?_102228231)_(105861009_?)dup	MOK, NUDT14 +47 more	Duplication	Herpes simplex encephalitis, susceptibility to, 3 +1 more	GUncertain significance
Select item 2424155	NC_000014.8:g.(?_102442029)_(105861009_?)del	ADSS1, AHNAK2 +46 more	Deletion	Charcot-Marie-Tooth disease axonal type 2O	GUncertain significance
Select item 1410807	NC_000014.8:g.(?_102229222)_(105861009_?)dup	ZFYVE21, ZNF839 +47 more	Duplication	not provided	GUncertain significance

ClinVar