LOC129996140[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	ABCF1, ABT1 +1340 more	Copy number gain	See cases	GPathogenic
Select item 144210	GRCh38/hg38 6p22.2-22.1(chr6:26280579-28727313)x3	ABT1, BTN1A1 +344 more	Copy number gain	See cases	GUncertain significance
Select item 3103703	NM_003510.3(H2AC15):c.316G>A (p.Gly106Ser)	H2AC15, LOC129996140 (G106S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283301	NM_003510.3(H2AC15):c.262A>G (p.Ile88Val)	H2AC15, LOC129996140 (I88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103702	NM_003510.3(H2AC15):c.235A>G (p.Ile79Val)	H2AC15, LOC129996140 (I79V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar