ClinVar for MedGen (Select 107884) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 523274	GRCh37/hg19 22q11.21(chr22:18894835-21505417)	CLTCL1, COMT +45 more	Copy number loss	Pes planus +13 more	GPathogenic
Select item 268010	46;XX;t(2;10)(p23;q22.1)dn		Translocation	Large for gestational age +9 more	GPathogenic
Select item 267914	46;XY;t(9;14)(p21;q12)dn		Translocation	Bilateral lung agenesis +9 more	GUncertain significance

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