ClinVar for Gene (Select 102465669) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2716360	NM_002496.4(NDUFS8):c.110-20C>G	MIR7113, NDUFS8	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1663446	NM_002496.4(NDUFS8):c.110-10C>T	MIR7113, NDUFS8	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 383040	NM_002496.4(NDUFS8):c.110-11C>T	MIR7113, NDUFS8	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +1 more	GLikely benign
Select item 153941	GRCh38/hg38 11q13.2-13.4(chr11:68031693-71593495)x1	LOC130006238, LOC130006239 +184 more	Copy number loss	See cases	GLikely pathogenic
Select item 146304	GRCh38/hg38 11q13.2-13.3(chr11:67217264-69448598)x1	ACY3, AIP +206 more	Copy number loss	See cases	GLikely pathogenic
Select item 58893	GRCh38/hg38 11q13.2(chr11:67446153-68679073)x1	ACY3, AIP +98 more	Copy number loss	See cases	GPathogenic

ClinVar