"GeneDx"[submitter] AND "FSIP2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58770	GRCh38/hg38 2q31.1-33.1(chr2:176304445-202039790)x1	LOC126806416, LOC126806417 +591 more	Copy number loss	See cases	GPathogenic
Select item 58771	GRCh38/hg38 2q31.2-33.1(chr2:177874070-198525492)x1	ANKAR, ANKRD44 +430 more	Copy number loss	See cases	GPathogenic
Select item 1702722	NM_173651.4(FSIP2):c.14054G>A (p.Cys4685Tyr)	FSIP2 (C4685Y)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance

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