"GeneDx"[submitter] AND "SPRY2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57644	GRCh38/hg38 13q22.3-32.1(chr13:78349126-94701844)x1	DCT, GPC5 +121 more	Copy number loss	See cases	GPathogenic
Select item 1259792	NM_005842.4(SPRY2):c.*107G>T	SPRY2	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 253533	GRCh37/hg19 13q21.33-31.2(chr13:72013791-88021559)x1	ACOD1, BORA +27 more	Copy number loss	See cases	GPathogenic
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic

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