"GeneDx"[submitter] AND "INPP4A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59145	GRCh38/hg38 2p11.2-q11.2(chr2:91443218-102334856)x3	ACTR1B, ADRA2B +331 more	Copy number gain	See cases	GPathogenic
Select item 152537	GRCh38/hg38 2q11.1-13(chr2:94678532-110602409)x3	ACTR1B, ADRA2B +550 more	Copy number gain	See cases	GPathogenic
Select item 59146	GRCh38/hg38 2q11.1-12.1(chr2:94817406-103252396)x3	LOC129934355, LOC129934356 +348 more	Copy number gain	See cases	GPathogenic
Select item 59147	GRCh38/hg38 2q11.2-13(chr2:97672522-110211318)x3	AFF3, C2orf15 +373 more	Copy number gain	See cases	GPathogenic
Select item 1254482	NM_001134225.2(INPP4A):c.2029-10G>C	INPP4A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3368764	NM_001134225.2(INPP4A):c.2687G>A (p.Arg896His)	INPP4A (R846H +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar