LOC121725061[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155448	GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3	LOC129931453, LOC129931454 +1585 more	Copy number gain	See cases	GPathogenic
Select item 58109	GRCh38/hg38 1q23.1-25.1(chr1:157747246-176021247)x3	ADAMTS4, ADCY10 +775 more	Copy number gain	See cases	GPathogenic
Select item 57465	GRCh38/hg38 1q23.2-24.1(chr1:159479887-166895086)x1	ADAMTS4, ALDH9A1 +371 more	Copy number loss	See cases	GPathogenic
Select item 57816	GRCh38/hg38 1q23.3(chr1:161513195-161671153)x3	FCGR2A, FCGR2B +13 more	Copy number gain	See cases	GUncertain significance
Select item 150542	GRCh38/hg38 1q23.3(chr1:161589951-161649210)x3	FCGR2B, FCGR2C +4 more	Copy number gain	See cases	GLikely benign
Select item 149428	GRCh38/hg38 1q23.3(chr1:161589951-161680659)x1	FCGR2B, FCGR2C +4 more	Copy number loss	See cases	GLikely benign
Select item 147039	GRCh38/hg38 1q23.3(chr1:161589976-161649084)x3	FCGR2B, FCGR2C +4 more	Copy number gain	See cases	GBenign

ClinVar