Related gene-specific medical variations for Gene (Select 64754) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1810325	GRCh37/hg19 1q44(chr1:246367970-246639585)x1	SMYD3	Copy number loss	not provided	Gnot provided
Select item 1808995	GRCh37/hg19 1q44(chr1:246174091-246702637)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 1808579	GRCh37/hg19 1q44(chr1:246037516-246465146)x4	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 1527714	GRCh37/hg19 1q44(chr1:246109449-246595110)	SMYD3	Copy number gain	not specified	GUncertain significance
Select item 1340896	GRCh37/hg19 1q44(chr1:245964948-246158491)x1	SMYD3	Copy number loss	not provided	GLikely benign
Select item 1340148	GRCh37/hg19 1q44(chr1:245904749-246056135)x1	SMYD3	Copy number loss	not provided	GLikely benign
Select item 1339908	GRCh37/hg19 1q44(chr1:246530458-246608001)x1	SMYD3	Copy number loss	not provided	Gnot provided
Select item 980429	GRCh37/hg19 1q44(chr1:246067928-246502233)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 980426	GRCh37/hg19 1q44(chr1:246174090-246701687)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 814202	GRCh37/hg19 1q44(chr1:246530458-246608001)x1	SMYD3	Copy number loss	not provided	GUncertain significance
Select item 814200	GRCh37/hg19 1q44(chr1:246193103-246688599)x1	SMYD3	Copy number loss	not provided	GLikely benign
Select item 814199	GRCh37/hg19 1q44(chr1:246174090-246674868)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 814198	GRCh37/hg19 1q44(chr1:246060750-246382096)x1	SMYD3	Copy number loss	not provided	GLikely benign
Select item 688793	GRCh37/hg19 1q44(chr1:246443511-246520363)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 688664	GRCh37/hg19 1q44(chr1:246163067-246583513)x1	SMYD3	Copy number loss	not provided	GUncertain significance
Select item 687323	GRCh37/hg19 1q44(chr1:246324759-246515943)x1	SMYD3	Copy number loss	not provided	GUncertain significance
Select item 687073	GRCh37/hg19 1q44(chr1:246163160-246700047)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 565255	GRCh37/hg19 1q44(chr1:246179294-246674868)x3	SMYD3	Copy number gain	not provided	GUncertain significance
Select item 442840	GRCh37/hg19 1q44(chr1:246352675-246624043)x1	SMYD3	Copy number loss	See cases	GLikely benign
Select item 393530	GRCh37/hg19 1q44(chr1:245900039-246475061)x1	SMYD3	Copy number loss	VATER association	GLikely benign
Select item 226135	GRCh37/hg19 1q44(chr1:246256444-246700236)	SMYD3	Copy number gain	Abnormal esophagus morphology	GLikely benign
Select item 145943	GRCh38/hg38 1q44(chr1:246386899-246415872)x1	SMYD3	Copy number loss	See cases	GLikely benign

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Links from Gene

Items: 22