Related gene-specific medical variations for Gene (Select 28513) - ClinVar - NCBI

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Links from Gene

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063555	GRCh37/hg19 18q22.1(chr18:64079710-64330253)x1	CDH19	Copy number loss	not specified	GUncertain significance
Select item 1526632	GRCh37/hg19 18q22.1(chr18:63892042-64657862)	CDH19	Copy number loss	not specified	GUncertain significance
Select item 979704	GRCh37/hg19 18q22.1(chr18:64143273-64202811)x1	CDH19	Copy number loss	not provided	GLikely benign
Select item 564522	GRCh37/hg19 18q22.1(chr18:63727661-64556147)x4	CDH19	Copy number gain	not provided	GUncertain significance
Select item 443764	GRCh37/hg19 18q22.1(chr18:64252800-64495798)x1	CDH19	Copy number loss	See cases	GLikely benign
Select item 441999	GRCh37/hg19 18q22.1(chr18:63998154-64504466)x1	CDH19	Copy number loss	See cases	GUncertain significance
Select item 394328	GRCh37/hg19 18q22.1(chr18:64123297-64316333)x1	CDH19	Copy number loss	See cases	GLikely benign
Select item 221763	GRCh38/hg38 18q22.1(chr18:66419523-66667666)x1	CDH19	Copy number loss	Premature ovarian failure	GBenign
Select item 154758	GRCh38/hg38 18q22.1(chr18:66242392-66790287)x1	CDH19	Copy number loss	See cases	GLikely benign
Select item 153572	GRCh38/hg38 18q22.1(chr18:66417411-66663016)x1	CDH19	Copy number loss	See cases	GLikely benign
Select item 153360	GRCh38/hg38 18q22.1(chr18:66594541-66837317)x1	CDH19	Copy number loss	See cases	GLikely benign
Select item 152855	GRCh38/hg38 18q22.1(chr18:66437554-66649096)x1	CDH19	Copy number loss	See cases	GUncertain significance
Select item 57463	GRCh38/hg38 18q22.1(chr18:66242508-66790270)x1	CDH19	Copy number loss	See cases	GUncertain significance