ClinVar (all) for Orgtrack (Select 505366) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 183388	NC_000023.9:g.146703942_146820448del	FMR1	Deletion	Fragile X syndrome	GPathogenic
Select item 183387	NM_002024.6(FMR1):c.-129CGG[201]	FMR1, FRAXA +2 more	Microsatellite (5 prime UTR variant +1 more)	Fragile X syndrome	GPathogenic
Select item 183386	chr17:g.(AC027266_AL353996)_(AC015726-AC087393)del		Deletion	Smith-Magenis syndrome	GPathogenic
Select item 183385	NC_000002.10:g.(148432391_148447295)_(148651456_148737275)del	LOC126806366, LOC126806367 +4 more	Deletion	Intellectual disability, autosomal dominant 1	GPathogenic
Select item 183384	NC_000002.10:g.146798229_150310317del		Deletion	Intellectual disability, autosomal dominant 1	GPathogenic
Select item 183383	NC_000002.10:g.148447496_149377297del	LOC129934890, LOC129934891 +15 more	Deletion	Intellectual disability, autosomal dominant 1	GPathogenic

ClinVar