"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "MIR6759 - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 583824	NC_000012.11:g.(?_58142298)_(58145510_?)dup	CDK4, LOC130008148 +2 more	Duplication	Familial melanoma	GUncertain significance
Select item 1491623	NM_000075.4(CDK4):c.820-3C>T	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GUncertain significance
Select item 1762451	NM_000075.4(CDK4):c.820-4T>G	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma +1 more	GConflicting classifications of pathogenicity
Select item 827505	NM_000075.4(CDK4):c.820-4T>C	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma +2 more	GLikely benign
Select item 1113929	NM_000075.4(CDK4):c.820-5C>T	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 532283	NM_000075.4(CDK4):c.820-5del	CDK4, MIR6759 +1 more	Deletion (non-coding transcript variant +2 more)	Familial melanoma	GUncertain significance
Select item 2880617	NM_000075.4(CDK4):c.820-6C>G	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 2117827	NM_000075.4(CDK4):c.820-7_820-6insG	CDK4, MIR6759 +1 more	Insertion (non-coding transcript variant +2 more)	Familial melanoma +1 more	GLikely benign
Select item 2198156	NM_000075.4(CDK4):c.820-8C>G	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 1152275	NM_000075.4(CDK4):c.820-8C>A	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 2811134	NM_000075.4(CDK4):c.820-10C>T	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 2865567	NM_000075.4(CDK4):c.820-13C>T	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 2120013	NM_000075.4(CDK4):c.820-13C>G	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 2017505	NM_000075.4(CDK4):c.820-14G>A	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma +1 more	GLikely benign
Select item 2727130	NM_000075.4(CDK4):c.820-15T>A	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 1660974	NM_000075.4(CDK4):c.820-15T>G	CDK4, MIR6759 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign
Select item 1576551	NM_000075.4(CDK4):c.820-15del	CDK4, MIR6759 +1 more	Deletion (non-coding transcript variant +2 more)	Familial melanoma	GLikely benign