Related gene-specific medical variations for Gene (Select 79582) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3168013	NM_024532.5(SPAG16):c.77C>T (p.Ala26Val)	LOC129935534, SPAG16 (A26V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221602	NM_024532.5(SPAG16):c.65G>T (p.Gly22Val)	LOC129935534, SPAG16 (G22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 979402	GRCh37/hg19 2q34(chr2:214021457-214324932)x3	SPAG16	Copy number gain	not provided	GUncertain significance
Select item 979401	GRCh37/hg19 2q34(chr2:214763339-214900967)x1	SPAG16	Copy number loss	not provided	GUncertain significance
Select item 816572	GRCh37/hg19 2q34(chr2:214906879-215068829)x1	SPAG16	Copy number loss	not provided	GLikely benign
Select item 814364	GRCh37/hg19 2q34(chr2:214769083-215110737)x3	SPAG16	Copy number gain	not provided	GLikely benign
Select item 686599	GRCh37/hg19 2q34(chr2:214981798-215049260)x1	SPAG16	Copy number loss	not provided	GUncertain significance
Select item 562558	GRCh37/hg19 2q34(chr2:214766288-215035184)x4	SPAG16	Copy number gain	not provided	GLikely benign
Select item 151430	GRCh38/hg38 2q34(chr2:214022722-214055178)x3	SPAG16	Copy number gain	See cases	GLikely benign

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