ClinVar for MedGen (Select 930195) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1707460	Single allele	CDHR2, EIF4E1B +71 more	Duplication	5q35 microduplication syndrome	GPathogenic
Select item 981214	GRCh37/hg19 5q35.1-35.3(chr5:170805664-180719789)x3	ADAMTS2, ARL10 +115 more	Copy number gain	5q35 microduplication syndrome	GPathogenic
Select item 830214	NC_000005.10:g.(177090796_177094455)_(177346090_177352856)dup	FGFR4, LMAN2 +4 more	Duplication	5q35 microduplication syndrome	GPathogenic

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