ClinVar for MedGen (Select 8649) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 267924	46;XY;t(16;20)(q23.1;p11.22)		Translocation	Sleep abnormality +24 more	GUncertain significance
Select item 267916	46;XY;t(10;14)(q11.2;q21)dn		Translocation	Specific learning disability +7 more	GUncertain significance
Select item 267887	46;XY;t(1;2)(p34.2;q35)dn		Translocation	Delayed speech and language development +9 more	GPathogenic
Select item 267834	46;X;t(Y;16)(q11.23;p11.2);t(6;21)(p21.3;p13)dn		Translocation	Specific learning disability +18 more	GLikely pathogenic
Select item 267829	46;XX;t(5;10)(p13.3;q21.1)dn		Translocation	Autistic behavior +10 more	GUncertain significance

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