ADGRL3-AS1[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57074	GRCh38/hg38 4p13-q13.1(chr4:44356201-62245882)x3	AASDH, ADGRL3 +244 more	Copy number gain	See cases	GPathogenic
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic
Select item 58028	GRCh38/hg38 4q12-13.2(chr4:51831622-66991489)x3	AASDH, ADGRL3 +177 more	Copy number gain	See cases	GPathogenic
Select item 1098574	GRCh38/hg38 4q12-21.1(chr4:51891814-76009719)x1	CDKL2, LOC110120745 +360 more	Copy number loss	Piebaldism	GPathogenic
Select item 59424	GRCh38/hg38 4q12-13.1(chr4:54198601-62270115)x1	AASDH, ADGRL3 +100 more	Copy number loss	See cases	GPathogenic
Select item 145654	GRCh38/hg38 4q13.1(chr4:61178277-62895417)x1	ADGRL3, ADGRL3-AS1 +8 more	Copy number loss	See cases	GLikely benign
Select item 154466	GRCh38/hg38 4q13.1(chr4:61356169-62527994)x3	ADGRL3, ADGRL3-AS1 +7 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 148106	GRCh38/hg38 4q13.1(chr4:62159937-62702902)x3	ADGRL3-AS1, LOC126807065 +5 more	Copy number gain	See cases	GBenign

ClinVar