Related gene-specific medical variations for Gene (Select 64579) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2689548	NM_022569.3(NDST4):c.2035C>T (p.Arg679Ter)	NDST4 (R679*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2685985	GRCh37/hg19 4q26(chr4:115760387-116288831)x3	NDST4	Copy number gain	not provided	GUncertain significance
Select item 980128	GRCh37/hg19 4q26(chr4:115928191-116099197)x1	NDST4	Copy number loss	not provided	GLikely benign
Select item 980127	GRCh37/hg19 4q26(chr4:115844816-116266652)x3	NDST4	Copy number gain	not provided	GLikely benign

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