"GenomeConnect, ClinGen"[submitter] AND "CD19"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1326293	GRCh38/hg38 16p11.2(chr16:28814284-29129367)x3	NFATC2IP-AS1, RABEP2 +36 more	Copy number gain	not provided	Gnot provided
Select item 318804	NM_001770.6(CD19):c.527C>T (p.Pro176Leu)	CD19 (P176L +1 more)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 3 +2 more	GUncertain significance
Select item 972938	GRCh37/hg19 16p12.2-11.2(chr16:21312200-29646379)x3	KDM8, LAT +69 more	Copy number gain	not provided	Gnot provided

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