ClinVar for Gene (Select 101927111) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155469	GRCh38/hg38 3p14.1(chr3:67561815-68974197)x1	LOC105377146, LOC108167314 +7 more	Copy number loss	See cases	Gconflicting data from submitters
Select item 150826	GRCh38/hg38 3p14.3-11.1(chr3:57140424-90259960)x1	HTD2, HTR1F +482 more	Copy number loss	See cases	GPathogenic
Select item 149610	GRCh38/hg38 3p14.1(chr3:67822085-68916513)x3	LOC105377146, LOC108167314 +3 more	Copy number gain	See cases	GUncertain significance
Select item 146408	GRCh38/hg38 3p14.1(chr3:67566837-68960045)x1	LOC105377146, LOC108167314 +7 more	Copy number loss	See cases	Gconflicting data from submitters
Select item 146339	GRCh38/hg38 3p14.1(chr3:67594927-68911377)x1	LOC105377146, LOC108167314 +7 more	Copy number loss	See cases	GUncertain significance
Select item 144339	GRCh38/hg38 3p14.1-13(chr3:67391006-73414001)x1	ARL6IP5, EBLN2 +142 more	Copy number loss	See cases	GPathogenic
Select item 57772	GRCh38/hg38 3p14.1-12.3(chr3:64761248-78410098)x1	ADAMTS9-AS2, ARL6IP5 +234 more	Copy number loss	See cases	GPathogenic
Select item 57136	GRCh38/hg38 3p14.2-14.1(chr3:61970847-68465832)x1	ADAMTS9, ADAMTS9-AS1 +106 more	Copy number loss	See cases	GPathogenic

ClinVar