Related gene-specific medical variations for Gene (Select 202559) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 442826	GRCh37/hg19 6q11.1(chr6:61928251-62912937)x3	KHDRBS2	Copy number gain	See cases	GLikely benign
Select item 441829	GRCh37/hg19 6q11.1(chr6:61886427-62921561)x3	KHDRBS2	Copy number gain	See cases	GUncertain significance
Select item 394513	GRCh37/hg19 6q11.1(chr6:62386147-62889604)x3	KHDRBS2	Copy number gain	See cases	GBenign
Select item 394493	GRCh37/hg19 6q11.1(chr6:62396147-62889604)x3	KHDRBS2	Copy number gain	See cases	GBenign
Select item 202239	GRCh37/hg19 6p11.2-q11.1(chr6:57590853-62891976)x3	KHDRBS2	Copy number gain	See cases	GLikely benign
Select item 155684	GRCh38/hg38 6q11.1(chr6:61916628-62161152)x1	KHDRBS2	Copy number loss	See cases	GUncertain significance
Select item 155624	GRCh38/hg38 6q11.1(chr6:61979668-62246665)x1	KHDRBS2	Copy number loss	See cases	GLikely benign
Select item 146540	GRCh38/hg38 6q11.1(chr6:61821881-62167348)x1	KHDRBS2	Copy number loss	See cases	GUncertain significance

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