102465133[Gene ID] - 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	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 59019	GRCh38/hg38 12q13.3-14.2(chr12:57013355-63042498)x1	AGAP2, AGAP2-AS1 +199 more	Copy number loss	See cases	GPathogenic
Select item 58212	GRCh38/hg38 12q14.1-14.2(chr12:60303553-63356583)x3	AVPR1A, LINC01465 +34 more	Copy number gain	See cases	GUncertain significance
Select item 150076	GRCh38/hg38 12q14.1-14.3(chr12:60907151-66568077)x1	AVPR1A, C12orf56 +144 more	Copy number loss	See cases	GPathogenic
Select item 155464	GRCh38/hg38 12q14.1(chr12:61201517-62266814)x3	LOC124629388, LOC126861552 +10 more	Copy number gain	See cases	GUncertain significance

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