ClinVar for MedGen (Select 343051) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 559402	Single allele	LOC130058361, LOC130058362 +10 more	Deletion	Secondary microcephaly +5 more	GUncertain significance
Select item 268039	46;XY;t(3;18)(q13.31;q22.1)dn		Translocation	Oligohydramnios +29 more	GPathogenic
Select item 268036	46;XX;t(2;10)(q22;22.3)dn		Translocation	Obesity +15 more	GPathogenic
Select item 268035	46;XX;t(19;21)(q13.3;q22.3)dn		Translocation	Pectus excavatum +22 more	GPathogenic
Select item 268014	46;XY;inv(2)(q11.2q33)dn		Inversion	Short palpebral fissure +9 more	GLikely pathogenic

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