ClinVar for Gene (Select 129995932) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113700	NM_001364614.2(KDM1B):c.2213G>A (p.Arg738Gln)	KDM1B, LOC129995932 (R506Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113699	NM_001364614.2(KDM1B):c.2186T>C (p.Val729Ala)	KDM1B, LOC129995932 (V497A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551115	NM_001364614.2(KDM1B):c.2207C>T (p.Thr736Met)	KDM1B, LOC129995932 (T736M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334818	NM_001364614.2(KDM1B):c.2174A>G (p.Asp725Gly)	KDM1B, LOC129995932 (D493G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	ILRUN-AS1, IP6K3 +2582 more	Copy number gain	See cases	GPathogenic
Select item 152197	GRCh38/hg38 6p23-22.3(chr6:14958760-18580908)x3	ATXN1, ATXN1-AS1 +162 more	Copy number gain	See cases	GUncertain significance
Select item 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	ABCF1, ABT1 +1340 more	Copy number gain	See cases	GPathogenic
Select item 58124	GRCh38/hg38 6p25.3-22.3(chr6:106431-18360595)x3	ADTRP, ATXN1 +825 more	Copy number gain	See cases	GPathogenic

ClinVar