Related gene-specific medical variations for Gene (Select 283417) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441030	NM_173812.5(DPY19L2):c.1816C>T (p.Arg606Cys)	DPY19L2 (R606C)	Single nucleotide variant (missense variant)	Spermatogenic failure 9	GUncertain significance
Select item 395672	GRCh37/hg19 12q14.2(chr12:63947732-64116509)x1	DPY19L2	Copy number loss	See cases	GLikely benign
Select item 221851	GRCh37/hg19 12q14.2(chr12:63946056-64116159)x3	DPY19L2	Copy number gain	Premature ovarian failure	GBenign
Select item 101507	NG_031909.1:g.(12232_26209)_(29173_47048)del	DPY19L2	Deletion	Spermatogenic failure 9	GPathogenic

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