"GeneDx"[submitter] AND "ADRB3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59766	GRCh38/hg38 8p23.1-11.1(chr8:12750796-43532444)x3	ADAM18, ADAM2 +922 more	Copy number gain	See cases	GPathogenic
Select item 59769	GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3	LOC130000309, LOC130000310 +900 more	Copy number gain	See cases	GPathogenic
Select item 59782	GRCh38/hg38 8p11.23-11.21(chr8:37899430-42371734)x3	ADAM18, ADAM2 +180 more	Copy number gain	See cases	GPathogenic
Select item 1264874	NM_000025.3(ADRB3):c.*250G>C	ADRB3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1244998	NM_000025.3(ADRB3):c.1206-96A>G	ADRB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288105	NM_000025.3(ADRB3):c.1205+307dup	ADRB3	Duplication (intron variant)	not provided	GBenign
Select item 1230608	NM_000025.3(ADRB3):c.1205+14G>T	ADRB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 17741	NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)	ADRB3 (W64R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 253803	GRCh37/hg19 8p11.23-11.22(chr8:37555526-38600788)x3	C8orf86, RAB11FIP1 +18 more	Copy number gain	See cases	GUncertain significance

ClinVar