"GeneDx"[submitter] AND "LOC128897170"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59131	GRCh38/hg38 2p25.3-24.3(chr2:30342-14866951)x3	ACP1, ADAM17 +413 more	Copy number gain	See cases	GPathogenic
Select item 1316851	NC_000002.12:g.10043421A>G	KLF11, LOC128897170	Single nucleotide variant	not provided	GLikely benign
Select item 1264076	NC_000002.12:g.10043428_10043438dup	KLF11, LOC128897170	Duplication	not provided	GBenign
Select item 1317869	NC_000002.12:g.10043500G>A	KLF11, LOC128897170	Single nucleotide variant	not provided	GLikely benign
Select item 1317896	NM_003597.5(KLF11):c.-157C>T	KLF11, LOC128897170	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 330619	NM_003597.5(KLF11):c.-95GCC[7]	LOC128897170, KLF11	Microsatellite (5 prime UTR variant)	Maturity onset diabetes mellitus in young +1 more	GConflicting classifications of pathogenicity
Select item 330618	NM_003597.5(KLF11):c.-95GCC[5]	KLF11, LOC128897170	Microsatellite (5 prime UTR variant)	not provided +1 more	GBenign

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