101928767[Gene ID] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155306	GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	LOC126862060, LOC126862061 +3282 more	Copy number gain	See cases	GPathogenic
Select item 146230	GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	LOC125048449, LOC125048450 +3277 more	Copy number gain	See cases	GPathogenic
Select item 144518	GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3	LOC130056651, LOC130056652 +1423 more	Copy number gain	See cases	GPathogenic
Select item 149176	GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3	ADCK1, ADSS1 +1204 more	Copy number gain	See cases	GPathogenic
Select item 148778	GRCh38/hg38 14q31.3(chr14:85536572-86997925)x3	FLRT2, LINC01148 +12 more	Copy number gain	See cases	GUncertain significance
Select item 146502	GRCh38/hg38 14q31.3(chr14:85815543-87531777)x3	LINC01148, LINC02296 +13 more	Copy number gain	See cases	GUncertain significance
Select item 157316	Single allele	LINC02316, LINC02328	Deletion	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 157317	Single allele	LINC02316, LINC02328	Deletion	Small for gestational age	Gnot provided
Select item 58526	GRCh38/hg38 14q31.3-32.33(chr14:86094030-106832642)x3	LOC130056392, LOC130056393 +1073 more	Copy number gain	See cases	GPathogenic

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