Related gene-specific medical variations for Gene (Select 64109) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376003	NM_022148.4(CRLF2):c.695T>G (p.Phe232Cys)	CRLF2 (F232C +1 more)	Single nucleotide variant (missense variant +1 more)	Lymphoblastic leukemia, acute, with lymphomatous features	GPathogenic
Select item 153133	GRCh38/hg38 Yp11.2(chrY:1000807-1223133)x1	CRLF2	Copy number loss	See cases	GLikely benign
Select item 151984	GRCh38/hg38 Yp11.2(chrY:1055101-1228390)x3	CRLF2	Copy number gain	See cases	GBenign
Select item 151870	GRCh38/hg38 Xp22.33(chrX:915816-1259698)x3	CRLF2	Copy number gain	See cases	GBenign
Select item 151815	GRCh38/hg38 Xp22.33(chrX:997890-1259698)x3	CRLF2	Copy number gain	See cases	GBenign/Likely benign
Select item 151798	GRCh38/hg38 Xp22.33(chrX:1055101-1228390)x3	CRLF2	Copy number gain	See cases	GBenign
Select item 151120	GRCh38/hg38 Xp22.33(chrX:1085618-1223133)x1	CRLF2	Copy number loss	See cases	GLikely benign
Select item 148362	GRCh38/hg38 Xp22.33(chrX:1000807-1223133)x1	CRLF2	Copy number loss	See cases	GLikely benign
Select item 145827	GRCh38/hg38 Xp22.33(chrX:1202712-1228390)x3	CRLF2	Copy number gain	See cases	GLikely benign
Select item 145803	GRCh38/hg38 Yp11.2(chrY:1123219-1202712)x3	CRLF2	Copy number gain	See cases	GBenign
Select item 145802	GRCh38/hg38 Xp22.33(chrX:1123219-1202712)x3	CRLF2	Copy number gain	See cases	GBenign
Select item 133950	NM_022148.4(CRLF2):c.730G>A (p.Val244Met)	CRLF2 (V132M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 133949	NM_022148.4(CRLF2):c.637G>A (p.Glu213Lys)	CRLF2 (E101K +1 more)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 133948	NM_022148.4(CRLF2):c.406G>A (p.Val136Met)	CRLF2 (V24M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 133947	NM_022148.4(CRLF2):c.190G>A (p.Gly64Ser)	CRLF2 (G64S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	Gnot provided
Select item 133946	NM_022148.4(CRLF2):c.269A>G (p.Gln90Arg)	CRLF2 (Q90R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	Gnot provided