Related gene-specific medical variations for Gene (Select 4745) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1527630	GRCh37/hg19 11p15.1(chr11:20821609-20875957)	NELL1	Copy number loss	not specified	GUncertain significance
Select item 1340164	GRCh37/hg19 11p15.1-14.3(chr11:21369308-21917565)x3	NELL1	Copy number gain	not provided	GUncertain significance
Select item 687387	GRCh37/hg19 11p15.1-14.3(chr11:21416074-21885376)x3	NELL1	Copy number gain	not provided	GUncertain significance
Select item 685681	GRCh37/hg19 11p15.1(chr11:20792281-21073130)x1	NELL1	Copy number loss	not provided	GUncertain significance
Select item 685646	GRCh37/hg19 11p15.1-14.3(chr11:21369307-21923060)x3	NELL1	Copy number gain	not provided	GUncertain significance
Select item 685434	GRCh37/hg19 11p15.1(chr11:21125532-21154364)x1	NELL1	Copy number loss	not provided	GUncertain significance
Select item 563834	GRCh37/hg19 11p15.1-14.3(chr11:21482932-21753111)x1	NELL1	Copy number loss	not provided	GUncertain significance
Select item 161645	NM_006157.5(NELL1):c.1666G>T (p.Gly556Ter)	NELL1 (G556* +2 more)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of prostate	GUncertain significance

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