ClinVar for Gene (Select 130064230) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140449	NM_001771.4(CD22):c.2416G>A (p.Asp806Asn)	CD22, LOC130064230 (D634N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526051	NM_001771.4(CD22):c.2455G>A (p.Gly819Arg)	CD22, LOC130064230 (G642R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219090	NM_001771.4(CD22):c.2452G>A (p.Glu818Lys)	CD22, LOC130064230 (E730K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 153499	GRCh38/hg38 19q12-13.12(chr19:31367353-35417098)x1	ANKRD27, CD22 +193 more	Copy number loss	See cases	GPathogenic
Select item 147631	GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	ALKBH6, ANKRD27 +439 more	Copy number loss	See cases	GPathogenic
Select item 146619	GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	ALKBH6, ANKRD27 +459 more	Copy number loss	See cases	GPathogenic
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic

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