ClinVar for Gene (Select 101929120) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154492	GRCh38/hg38 1q31.1-31.2(chr1:189460972-190945450)x3	BRINP3, BRINP3-DT +20 more	Copy number gain	See cases	GLikely benign
Select item 154301	GRCh38/hg38 1q24.3-31.2(chr1:170929720-191065409)x1	LOC129932082, LOC129932083 +561 more	Copy number loss	See cases	GPathogenic
Select item 152129	GRCh38/hg38 1q31.1-31.2(chr1:190036204-190945450)x1	BRINP3, BRINP3-DT +13 more	Copy number loss	See cases	GUncertain significance
Select item 146340	GRCh38/hg38 1q31.1(chr1:189593085-190776678)x1	BRINP3, BRINP3-DT +19 more	Copy number loss	See cases	GLikely benign
Select item 146285	GRCh38/hg38 1q31.1-32.1(chr1:189034483-199615866)x1	ASPM, ATP6V1G3 +173 more	Copy number loss	See cases	GPathogenic
Select item 144717	GRCh38/hg38 1q25.2-31.3(chr1:176595962-196301688)x1	MIR488, MR1 +456 more	Copy number loss	See cases	GPathogenic
Select item 60076	GRCh38/hg38 1q25.2-32.1(chr1:179032905-199724897)x1	LOC129932021, LOC129932022 +478 more	Copy number loss	See cases	GPathogenic
Select item 58112	GRCh38/hg38 1q31.1-42.11(chr1:187143981-224299417)x3	LOC129932539, LOC129932540 +1148 more	Copy number gain	See cases	GPathogenic

ClinVar