CSTF3-DT[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154432	GRCh38/hg38 11p15.1-13(chr11:20079474-34463996)x1	ABTB2, ANO3 +283 more	Copy number loss	See cases	GPathogenic
Select item 58858	GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1	PAX6_HS3, PAX6_HS8 +334 more	Copy number loss	See cases	GPathogenic
Select item 145969	GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1	LOC129390275, LOC129390276 +255 more	Copy number loss	See cases	GPathogenic
Select item 147329	GRCh38/hg38 11p13(chr11:32986646-33573778)x3	CSTF3, CSTF3-DT +26 more	Copy number gain	See cases	GUncertain significance
Select item 56995	GRCh38/hg38 11p13(chr11:33031527-33620145)x3	CSTF3, CSTF3-DT +22 more	Copy number gain	See cases	GUncertain significance

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