"Invitae"[submitter] AND "CD276"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 750335	NM_001024736.2(CD276):c.734-10C>T	CD276	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 722881	NM_001024736.2(CD276):c.734-7C>T	CD276	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 779896	NM_001024736.2(CD276):c.1257G>A (p.Leu419=)	CD276	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2427095	NC_000015.9:g.(?_72978569)_(75190071_?)dup	ADPGK, ARID3B +29 more	Duplication	Bardet-Biedl syndrome	GUncertain significance
Select item 1458323	NC_000015.9:g.(?_72103084)_(74244178_?)del	ADPGK, ARIH1 +19 more	Deletion	Tay-Sachs disease	GPathogenic
Select item 1353978	NC_000015.9:g.(?_72978569)_(75722716_?)del	ADPGK, ARID3B +41 more	Deletion	not provided	GPathogenic
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	ALDH1A2, ALPK3 +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance

ClinVar