ClinVar for Gene (Select 154092) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155377	GRCh38/hg38 6q23.2-27(chr6:133537271-165875545)x3	LOC129997450, LOC129997451 +1002 more	Copy number gain	See cases	GPathogenic
Select item 150937	GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3	LOC129996876, LOC129996877 +1449 more	Copy number gain	See cases	GPathogenic
Select item 144758	GRCh38/hg38 6q23.2-23.3(chr6:134143117-134707402)x3	CT69, LINC01010 +18 more	Copy number gain	See cases	GUncertain significance

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