ClinVar for MedGen (Select 868200) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1330179	GRCh37/hg19 9q33.1-33.2(chr9:117853848-124633077)x1	ASTN2, BRINP1 +19 more	Copy number loss	Intellectual disability, borderline +5 more	GUncertain significance
Select item 267882	46;XX;inv(7)(q11.23q36.3)dn		Inversion	Congenital finger flexion contractures +13 more	GPathogenic
Select item 267876	46;XY;t(2;6)(q32.3;q25.3)dn		Translocation	Growth delay +3 more	GLikely pathogenic

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