Related gene-specific medical variations for Gene (Select 117154) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807605	GRCh37/hg19 Xq21.2(chrX:85478159-85630999)x0	DACH2	Copy number loss	not provided	GUncertain significance
Select item 979833	GRCh37/hg19 Xq21.2-21.31(chrX:85631053-86633326)x3	DACH2	Copy number gain	not provided	GUncertain significance
Select item 685924	GRCh37/hg19 Xq21.2-21.31(chrX:85632464-86639781)x2	DACH2	Copy number gain	not provided	GUncertain significance
Select item 685697	GRCh37/hg19 Xq21.2-21.31(chrX:85630983-86642342)x3	DACH2	Copy number gain	not provided	GUncertain significance
Select item 564865	GRCh37/hg19 Xq21.2-21.31(chrX:85632742-86633326)x2	DACH2	Copy number gain	not provided	GUncertain significance
Select item 564864	GRCh37/hg19 Xq21.2(chrX:85588096-86011611)x0	DACH2	Copy number loss	not provided	GLikely benign

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