Related gene-specific medical variations for Gene (Select 8945) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2058547	NM_033637.4(BTRC):c.37C>A (p.Leu13Ile)	BTRC, LOC130004556 (L13I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 979287	GRCh37/hg19 10q24.32(chr10:103024290-103254047)x3	BTRC	Copy number gain	not provided	GUncertain significance
Select item 563713	GRCh37/hg19 10q24.32(chr10:103130625-103323554)x3	BTRC	Copy number gain	not provided	GUncertain significance
Select item 154969	GRCh38/hg38 10q24.32(chr10:101528554-101556158)x3	BTRC	Copy number gain	See cases	GUncertain significance
Select item 148790	GRCh38/hg38 10q24.32(chr10:101528556-101562006)x3	BTRC	Copy number gain	See cases	GLikely benign

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