"GeneDx"[submitter] AND "GRWD1"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59115	GRCh38/hg38 19q13.32-13.33(chr19:46658791-49050450)x3	LOC130064822, LOC130064823 +290 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 1278331	NM_031485.4(GRWD1):c.956G>A (p.Arg319Gln)	GRWD1 (R319Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 253887	GRCh37/hg19 19q13.33(chr19:48876760-49053557)x3	KDELR1, GRIN2D +5 more	Copy number gain	See cases	GUncertain significance

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