Related gene-specific medical variations for Gene (Select 256435) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1527104	GRCh37/hg19 1p31.1(chr1:76616979-76917300)	ST6GALNAC3	Copy number gain	not specified	GUncertain significance
Select item 814103	GRCh37/hg19 1p31.1(chr1:76755334-77111467)x3	ST6GALNAC3	Copy number gain	not provided	GUncertain significance
Select item 814102	GRCh37/hg19 1p31.1(chr1:76754742-77126189)x3	ST6GALNAC3	Copy number gain	not provided	GUncertain significance
Select item 565116	GRCh37/hg19 1p31.1(chr1:77037368-77149014)x1	ST6GALNAC3	Copy number loss	not provided	GUncertain significance
Select item 565115	GRCh37/hg19 1p31.1(chr1:76731026-77317258)x3	ST6GALNAC3	Copy number gain	not provided	GUncertain significance
Select item 524187	t(1;4)(p21;p11)dn	CPEB2, ST6GALNAC3	Translocation	not specified	GUncertain significance
Select item 425536	GRCh37/hg19 1p31.1(chr1:76695673-76849907)x1	ST6GALNAC3	Copy number loss	not provided	GLikely benign
Select item 394492	GRCh37/hg19 1p31.1(chr1:76575130-76671617)x3	ST6GALNAC3	Copy number gain	See cases	GLikely benign
Select item 152758	GRCh38/hg38 1p31.1(chr1:76285095-76419302)x3	ST6GALNAC3	Copy number gain	See cases	GUncertain significance

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