"GeneDx"[submitter] AND "TMPRSS2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145984	GRCh38/hg38 21q22.11-22.3(chr21:7749532-46670346)x3	AATBC, ABCG1 +1159 more	Copy number gain	See cases	GPathogenic
Select item 1257425	NM_005656.4(TMPRSS2):c.478G>A (p.Val160Met)	TMPRSS2 (V160M +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1273671	NM_005656.4(TMPRSS2):c.-57+99G>T	LOC117134604, TMPRSS2 (G8V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 253512	GRCh37/hg19 21q11.2-22.3(chr21:15538655-48080926)x1	ABCG1, ADAMTS1 +216 more	Copy number loss	See cases	GPathogenic
Select item 253477	GRCh37/hg19 21q22.2-22.3(chr21:39841248-44652723)x3	PKNOX1, TMPRSS3 +37 more	Copy number gain	See cases	GPathogenic
Select item 253403	GRCh37/hg19 21q11.2-22.3(chr21:15410701-48090317)x3	ABCG1, ADAMTS1 +216 more	Copy number gain	See cases	GPathogenic

ClinVar