LOC126805813[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146350	GRCh38/hg38 1p31.1-21.1(chr1:83457325-104273917)x3	LOC126805769, LOC126805770 +548 more	Copy number gain	See cases	GPathogenic
Select item 146007	GRCh38/hg38 1p21.3-13.3(chr1:97272349-108893138)x1	AGL, AKNAD1 +194 more	Copy number loss	See cases	GPathogenic
Select item 60005	GRCh38/hg38 1p21.3-13.3(chr1:97410602-110670510)x1	AGL, AHCYL1 +332 more	Copy number loss	See cases	GPathogenic
Select item 60007	GRCh38/hg38 1p21.2-13.2(chr1:101618097-111703028)x1	ELAPOR1, EPS8L3 +276 more	Copy number loss	See cases	GPathogenic
Select item 149881	GRCh38/hg38 1p21.1(chr1:102191079-102384277)x1	LOC126805813	Copy number loss	See cases	GLikely benign
Select item 144810	GRCh38/hg38 1p21.1(chr1:102191098-102384167)x1	LOC126805813	Copy number loss	See cases	GBenign
Select item 156744	Single allele	LOC126805813	Deletion	Small for gestational age	Gnot provided
Select item 221684	GRCh38/hg38 1p21.1(chr1:102207943-102378169)x1	LOC126805813	Copy number loss	Premature ovarian failure	GBenign

ClinVar