"GeneDx"[submitter] AND "WDR37"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58710	GRCh38/hg38 10p15.3-15.1(chr10:69260-6209368)x1	ADARB2, ADARB2-AS1 +276 more	Copy number loss	See cases	GPathogenic
Select item 59657	GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	LOC126860819, LOC126860820 +680 more	Copy number gain	See cases	GPathogenic
Select item 146014	GRCh38/hg38 10p15.3-13(chr10:73856-12815915)x3	LOC132090805, MANCR +482 more	Copy number gain	See cases	GPathogenic
Select item 58711	GRCh38/hg38 10p15.3(chr10:87458-2482736)x1	ADARB2, ADARB2-AS1 +66 more	Copy number loss	See cases	GPathogenic
Select item 57853	GRCh38/hg38 10p15.3(chr10:730608-1358880)x3	ADARB2, GTPBP4 +27 more	Copy number gain	See cases	GUncertain significance
Select item 1031227	NM_014023.4(WDR37):c.344C>T (p.Thr115Ile)	WDR37 (T115I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1199795	NM_014023.4(WDR37):c.373A>G (p.Thr125Ala)	WDR37 (T125A)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 2571986	NM_014023.4(WDR37):c.485T>G (p.Val162Gly)	WDR37 (V162G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1311653	NM_014023.4(WDR37):c.694C>G (p.Leu232Val)	LOC126860809, WDR37 (L232V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2443495	NM_014023.4(WDR37):c.740A>G (p.Asp247Gly)	WDR37 (D247G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1707761	NM_014023.4(WDR37):c.800G>C (p.Cys267Ser)	WDR37 (C267S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2136232	NM_014023.4(WDR37):c.920T>C (p.Leu307Pro)	WDR37 (L307P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2505873	NM_014023.4(WDR37):c.934A>T (p.Thr312Ser)	WDR37 (T312S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1314600	NM_014023.4(WDR37):c.1073A>C (p.His358Pro)	WDR37 (H358P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1306370	NM_014023.4(WDR37):c.1217G>A (p.Arg406His)	WDR37 (R406H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2428810	NM_014023.4(WDR37):c.1367T>C (p.Met456Thr)	WDR37 (M456T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance