"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "NBR2"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 209582	NC_000017.11:g.43126099T>C	NBR2, BRCA1 +1 more	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 209583	NC_000017.11:g.43126360G>A	BRCA1, LOC111589215 +1 more	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 1	GBenign
Select item 3243158	NC_000017.10:g.(?_41277268)_(41836109_?)dup	ARL4D, BRCA1 +7 more	Duplication	not provided	GUncertain significance
Select item 3243027	NC_000017.10:g.(?_41249295)_(41320078_?)dup	BRCA1, NBR2	Duplication	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 3242979	NC_000017.10:g.(?_41277346)_(41278211_?)del	BRCA1, NBR2	Deletion	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 2425726	NC_000017.10:g.(?_41267778)_(41280110_?)del	BRCA1, NBR2	Deletion	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 831192	NC_000017.11:g.(?_43047633)_(43126360_?)del	BRCA1, NBR2	Deletion	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 584346	NC_000017.10:g.(?_41276016)_(41635727_?)dup	ARL4D, BRCA1 +5 more	Duplication	Hereditary breast ovarian cancer syndrome	GUncertain significance

ClinVar