C0456070[trait identifier] AND "Talkowski Laboratory, Center for Human - ClinVar

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	Variation	Type (Consequence)	Condition	Classification, Review status
Select item 267945	46;XY;t(1;18)(q32.1;q22.1)	Translocation	Mild global developmental delay +5 more	GUncertain significance
Select item 267943	46;XX;t(4;13)(q31.3;q14.3)dn	Translocation	Decreased body weight +7 more	GUncertain significance
Select item 267910	46;XX;t(11;17)(q13;q25)dn	Translocation	Tibial torsion +7 more	GUncertain significance
Select item 267896	46;XX;t(2;8)(q33;p21)dn	Translocation	EEG abnormality +5 more	GLikely pathogenic
Select item 267885	46;XY;t(2;6)(q33;q21)dn	Translocation	Intellectual disability +7 more	GPathogenic
Select item 267876	46;XY;t(2;6)(q32.3;q25.3)dn	Translocation	Growth delay +3 more	GLikely pathogenic
Select item 267867	46;XX;t(6;15)(q23;q22)dn	Translocation	Speech articulation difficulties +12 more	GLikely pathogenic
Select item 267857	46;XX;inv(5)(q14q35)dn	Inversion	Global developmental delay +14 more	GPathogenic
Select item 267850	46;XY;t(8;10)(q13;p13)dn	Translocation	Global developmental delay +13 more	GPathogenic
Select item 267833	46;XY;t(6;12)(q14;q24);20p+dn	Complex	Unilateral renal agenesis +14 more	GPathogenic
Select item 267830	46;X;t(X;5)(q24;q13)dn	Translocation	Growth delay +20 more	GPathogenic
Select item 267821	46;XX;t(3;12)(q13.2;q14)dn	Translocation	Thin upper lip vermilion +16 more	GPathogenic
Select item 267820	46;XY;t(16;20)(q11.2;q13.2)dn	Translocation	Atrial septal defect +10 more	GUncertain significance