Related gene-specific medical variations for Gene (Select 23362) - ClinVar

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Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685303	GRCh37/hg19 8p22(chr8:18572341-18814398)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 2685302	GRCh37/hg19 8p22(chr8:18502293-18603518)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 1341283	GRCh37/hg19 8p22-21.3(chr8:18753838-19044726)x3	PSD3	Copy number gain	not provided	GUncertain significance
Select item 980304	GRCh37/hg19 8p22(chr8:18729346-18814062)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 689253	GRCh37/hg19 8p22(chr8:18641302-18669765)x3	PSD3	Copy number gain	not provided	GUncertain significance
Select item 688809	GRCh37/hg19 8p22-21.3(chr8:18753362-19000923)x3	PSD3	Copy number gain	not provided	GUncertain significance
Select item 685337	GRCh37/hg19 8p22(chr8:18749192-18834806)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 563457	GRCh37/hg19 8p22(chr8:18539767-18753378)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 563451	GRCh37/hg19 8p22(chr8:18669679-18869618)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 563448	GRCh37/hg19 8p22(chr8:18316992-18492779)x1	PSD3	Copy number loss	not provided	GLikely benign
Select item 563440	GRCh37/hg19 8p22(chr8:18437638-18543814)x1	PSD3	Copy number loss	not provided	GUncertain significance
Select item 395529	GRCh37/hg19 8p22(chr8:18725030-18888257)x3	PSD3	Copy number gain	See cases	GUncertain significance