"GeneDx"[submitter] AND "MKI67"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 58821	GRCh38/hg38 10q26.13-26.2(chr10:122973296-128210291)x1	ABRAXAS2, ACADSB +182 more	Copy number loss	See cases	GPathogenic
Select item 152830	GRCh38/hg38 10q26.13-26.3(chr10:125452905-133785874)x3	ADAM12, ADAM8 +241 more	Copy number gain	See cases	GPathogenic
Select item 58823	GRCh38/hg38 10q26.2-26.3(chr10:126256585-133613938)x1	ADAM12, ADAM8 +207 more	Copy number loss	See cases	GPathogenic
Select item 57914	GRCh38/hg38 10q26.2-26.3(chr10:127852284-129780378)x3	AS-PTPRE, CLRN3 +32 more	Copy number gain	See cases	GUncertain significance
Select item 1274348	NM_002417.5(MKI67):c.8158A>C (p.Thr2720Pro)	MKI67 (T2360P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1294561	NM_002417.5(MKI67):c.7946G>A (p.Arg2649His)	MKI67 (R2289H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1228020	NM_002417.5(MKI67):c.5187C>T (p.Asn1729=)	MKI67	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic

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