ClinVar for MedGen (Select 856021) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1810323	GRCh37/hg19 Xq26.3(chrX:136647475-136892054)x3	ZIC3	Copy number gain	X-linked acrogigantism due to Xq26 microduplication	Gnot provided
Select item 374412	Single allele	ARHGEF6, CD40LG +3 more	Duplication	X-linked acrogigantism due to Xq26 microduplication	GLikely pathogenic
Select item 374411	Single allele	ARHGEF6, BRS3 +5 more	Duplication	X-linked acrogigantism due to Xq26 microduplication	GLikely pathogenic
Select item 374410	Single allele	ARHGEF6, CD40LG +3 more	Duplication	X-linked acrogigantism due to Xq26 microduplication	GLikely pathogenic
Select item 374409	Single allele	ARHGEF6, BRS3 +5 more	Duplication	X-linked acrogigantism due to Xq26 microduplication	GLikely pathogenic
Select item 243065	Single allele	RBMX, GPR101 +3 more	Duplication	X-linked acrogigantism due to Xq26 microduplication	GPathogenic
Select item 224866	GRCh37/hg19 Xq26.3(chrX:135602028-136259908)x2	CD40LG, VGLL1 +3 more	Copy number gain	X-linked acrogigantism due to Xq26 microduplication	GPathogenic

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