ClinVar for Gene (Select 283089) - ClinVar - NCBI

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Links from Gene

Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1289331	NC_000010.11:g.120851127T>G	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1280580	NC_000010.11:g.120851134A>C	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1261778	NC_000010.11:g.120851145T>C	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1233113	NC_000010.11:g.120850879C>G	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1211816	NC_000010.11:g.120850918C>T	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 1190555	NC_000010.11:g.120851124G>A	WDR11, WDR11-DT	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 153718	GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3	LOC130004884, LOC130004885 +438 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 148437	GRCh38/hg38 10q25.2-26.12(chr10:112701186-120970617)x3	LOC126861050, LOC126861051 +248 more	Copy number gain	See cases	GLikely pathogenic
Select item 144206	GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	LOC126861107, LOC128598885 +802 more	Copy number gain	See cases	GPathogenic
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 57507	GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	ABLIM1, ABRAXAS2 +679 more	Copy number gain	See cases	GPathogenic
Select item 57403	GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1	LOC130004881, LOC130004882 +418 more	Copy number loss	See cases	GPathogenic
Select item 57088	GRCh38/hg38 10q26.11-26.13(chr10:119273012-123117390)x3	FGFR2, GRK5 +119 more	Copy number gain	See cases	GPathogenic