Related gene-specific medical variations for Gene (Select 133022) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 814603	GRCh37/hg19 4q26(chr4:117624138-118017424)x3	TRAM1L1	Copy number gain	not provided	GLikely benign
Select item 814602	GRCh37/hg19 4q26(chr4:117071980-118177853)x1	TRAM1L1	Copy number loss	not provided	GLikely benign
Select item 562961	GRCh37/hg19 4q26(chr4:117587400-118681955)x1	TRAM1L1	Copy number loss	not provided	GUncertain significance
Select item 442209	GRCh37/hg19 4q26(chr4:117734128-118284598)x3	TRAM1L1	Copy number gain	See cases	GUncertain significance
Select item 441819	GRCh37/hg19 4q26(chr4:117071980-118163551)x1	TRAM1L1	Copy number loss	See cases	GUncertain significance
Select item 395648	GRCh37/hg19 4q26(chr4:117824501-118593760)x3	TRAM1L1	Copy number gain	See cases	GLikely benign

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