Related gene-specific medical variations for Gene (Select 1010) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685149	GRCh37/hg19 5p14.3(chr5:21122431-22521043)x1	CDH12	Copy number loss	not provided	GUncertain significance
Select item 2684411	GRCh37/hg19 5p14.3(chr5:21643506-22003203)x3	CDH12	Copy number gain	not provided	GUncertain significance
Select item 1809038	GRCh37/hg19 5p14.3(chr5:21740926-21792313)x1	CDH12	Copy number loss	not provided	GUncertain significance
Select item 1808561	GRCh37/hg19 5p14.3(chr5:21633198-22012296)x3	CDH12	Copy number gain	not provided	GUncertain significance
Select item 1807782	GRCh37/hg19 5p14.3(chr5:22130874-22556566)x1	CDH12	Copy number loss	not provided	GUncertain significance
Select item 814674	GRCh37/hg19 5p14.3(chr5:22284859-22762721)x1	CDH12	Copy number loss	not provided	GUncertain significance
Select item 814672	GRCh37/hg19 5p14.3(chr5:21528584-21845788)x3	CDH12	Copy number gain	not provided	GUncertain significance
Select item 814670	GRCh37/hg19 5p14.3(chr5:20002584-22393176)x3	CDH12	Copy number gain	not provided	GUncertain significance
Select item 563052	GRCh37/hg19 5p14.3(chr5:22770421-23082328)x3	CDH12	Copy number gain	not provided	GUncertain significance
Select item 446362	GRCh37/hg19 5p14.3(chr5:22657926-23156895)x3	CDH12	Copy number gain	See cases	GUncertain significance