FAM138F[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151484	GRCh38/hg38 19p13.3(chr19:61112-186241)x3	FAM138F, MIR1302-11 +1 more	Copy number gain	See cases	GBenign
Select item 151472	GRCh38/hg38 19p13.3(chr19:61112-127601)x3	FAM138F, MIR1302-11 +1 more	Copy number gain	See cases	GLikely benign
Select item 145254	GRCh38/hg38 19p13.3(chr19:61112-202952)x3	FAM138F, LINC01002 +2 more	Copy number gain	See cases	GBenign
Select item 145092	GRCh38/hg38 19p13.3(chr19:61112-113418)x1	FAM138F, MIR1302-11 +1 more	Copy number loss	See cases	GBenign
Select item 145091	GRCh38/hg38 19p13.3(chr19:61112-113418)x3	FAM138F, MIR1302-11 +1 more	Copy number gain	See cases	GBenign
Select item 145081	GRCh38/hg38 19p13.3(chr19:61112-168688)x3	FAM138F, MIR1302-11 +1 more	Copy number gain	See cases	GBenign
Select item 145085	GRCh38/hg38 19p13.3(chr19:74459-113418)x1	FAM138F, OR4F17	Copy number loss	See cases	GBenign
Select item 145084	GRCh38/hg38 19p13.3(chr19:74459-113418)x3	FAM138F, OR4F17	Copy number gain	See cases	GBenign

ClinVar