ClinVar for Gene (Select 105370888) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3179126	NM_001080462.3(TMEM202):c.791A>G (p.Lys264Arg)	TMEM202, TMEM202-AS1 (K264R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3179125	NM_001080462.3(TMEM202):c.719C>T (p.Pro240Leu)	TMEM202, TMEM202-AS1 (P240L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	LOC116268473, LOC116268474 +1244 more	Copy number gain	See cases	GPathogenic
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 153193	GRCh38/hg38 15q23-25.1(chr15:70025300-78705993)x1	ACSBG1, ADPGK +487 more	Copy number loss	See cases	GPathogenic
Select item 147526	GRCh38/hg38 15q23-24.1(chr15:72366869-72671688)x1	ARIH1, GOLGA6B +15 more	Copy number loss	See cases	GUncertain significance
Select item 58353	GRCh38/hg38 15q23-24.1(chr15:72058544-72481033)x3	ARIH1, CELF6 +33 more	Copy number gain	See cases	GUncertain significance
Select item 57140	GRCh38/hg38 15q23-24.1(chr15:68830574-73823337)x1	ADPGK, ADPGK-AS1 +197 more	Copy number loss	See cases	GPathogenic

ClinVar