ClinVar for Gene (Select 54435) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2405341	NR_002139.2(HCG4):n.871G>A	HCG4, LOC554223	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2254866	NR_002139.2(HCG4):n.424T>G	HCG4, LOC554223	Single nucleotide variant (non-coding transcript 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 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	ABCF1, ABT1 +1340 more	Copy number gain	See cases	GPathogenic

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