LOC126861589[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	LOC130008916, LOC130008917 +4836 more	Copy number gain	See cases	GPathogenic
Select item 155032	GRCh38/hg38 12q21.1-22(chr12:73485697-92795805)x1	ACSS3, ALX1 +287 more	Copy number loss	See cases	GPathogenic
Select item 153986	GRCh38/hg38 12q21.31(chr12:85578345-85815687)x1	LOC126861588, LOC126861589 +1 more	Copy number loss	See cases	GUncertain significance
Select item 151291	GRCh38/hg38 12q21.31(chr12:85584352-85784283)x1	LOC126861588, LOC126861589	Copy number loss	See cases	GUncertain significance
Select item 155425	GRCh38/hg38 12q21.31-21.32(chr12:85722164-86332192)x3	LOC126861589, LOC130008342 +3 more	Copy number gain	See cases	GLikely benign

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