Related gene-specific medical variations for Gene (Select 9223) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062721	GRCh37/hg19 3p14.1(chr3:65510176-66372903)x3	MAGI1	Copy number gain	not specified	GUncertain significance
Select item 1809011	GRCh37/hg19 3p14.1(chr3:65489460-65780869)x1	MAGI1	Copy number loss	not provided	GUncertain significance
Select item 1340768	GRCh37/hg19 3p14.1(chr3:65557424-65753176)x1	MAGI1	Copy number loss	not provided	GUncertain significance
Select item 687178	GRCh37/hg19 3p14.1(chr3:65501386-66372903)x4	MAGI1	Copy number gain	not provided	GUncertain significance
Select item 687090	GRCh37/hg19 3p14.1(chr3:65971545-66094088)x3	MAGI1	Copy number gain	not provided	GUncertain significance
Select item 562780	GRCh37/hg19 3p14.1(chr3:65609952-65661896)x1	MAGI1	Copy number loss	not provided	GLikely benign
Select item 562779	GRCh37/hg19 3p14.1(chr3:65502771-66378999)x3	MAGI1	Copy number gain	not provided	GUncertain significance
Select item 151736	GRCh38/hg38 3p14.1(chr3:65536355-65582844)x3	MAGI1	Copy number gain	See cases	GLikely benign

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