"GeneDx"[submitter] AND "ABCG2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic
Select item 59455	GRCh38/hg38 4q21.21-22.1(chr4:79575748-92412449)x1	ABCG2, ABRAXAS1 +251 more	Copy number loss	See cases	GPathogenic
Select item 152923	GRCh38/hg38 4q21.23-22.2(chr4:85449365-93973194)x1	ABCG2, AFF1 +126 more	Copy number loss	See cases	GPathogenic
Select item 1251382	NC_000004.12:g.88089831A>G	ABCG2	Single nucleotide variant	not provided	GBenign
Select item 1239257	NM_004827.3(ABCG2):c.1277+2227G>A	ABCG2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267736	NM_004827.3(ABCG2):c.1277+1908T>G	ABCG2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265403	NM_004827.3(ABCG2):c.1195-834T>G	ABCG2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236609	NM_004827.3(ABCG2):c.-20+6341T>G	ABCG2	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar