10[chr] AND 89623000:89730000[chrpos37] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 661198	NC_000010.11:g.(?_86755016)_(87965482_?)del	LOC111982877, LOC111982878 +61 more	Deletion	Generalized juvenile polyposis/juvenile polyposis coli	GPathogenic
Select item 646972	NC_000010.11:g.(?_86838866)_(87965482_?)del	ADIRF, ADIRF-AS1 +60 more	Deletion	Generalized juvenile polyposis/juvenile polyposis coli	GPathogenic
Select item 660158	NC_000010.11:g.(?_86875868)_(87894129_?)del	LOC130004268, LOC130004269 +57 more	Deletion	PTEN hamartoma tumor syndrome	GPathogenic
Select item 583889	NC_000010.10:g.(?_89622918)_(89624325_?)dup	KLLN, LOC130004273 +2 more	Duplication	PTEN hamartoma tumor syndrome	GUncertain significance
Select item 584299	NC_000010.11:g.(?_87863171)_(87864558_?)del	KLLN, LOC130004273 +2 more	Deletion	PTEN hamartoma tumor syndrome	GPathogenic
Select item 1771406	NM_000314.4(PTEN):c.-1032-222_-366del889	LOC130004273, LOC130004274 +2 more	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488867	NM_001126049.2(KLLN):c.-756T>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488868	NM_001126049.2(KLLN):c.-758G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 2682053	NM_001126049.2(KLLN):c.-759del	KLLN, PTEN	Deletion (5 prime UTR variant)	not provided	GUncertain significance
Select item 488935	NM_001126049.2(KLLN):c.-760del	KLLN, PTEN	Deletion (5 prime UTR variant)	not provided	GUncertain significance
Select item 488954	NM_001126049.2(KLLN):c.-761C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488773	NM_001126049.2(KLLN):c.-761C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 186991	NM_001126049.2(KLLN):c.-766G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 142999	NM_001126049.2(KLLN):c.-768A>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488850	NM_001126049.2(KLLN):c.-770C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1750483	NM_001126049.2(KLLN):c.-771G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 189521	NM_001126049.2(KLLN):c.-772G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 189469	NM_001126049.2(KLLN):c.-774G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 234396	NM_001126049.2(KLLN):c.-775C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488714	NM_001126049.2(KLLN):c.-776G>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488715	NM_001126049.2(KLLN):c.-777C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided +5 more	GUncertain significance
Select item 234473	NM_001126049.2(KLLN):c.-780C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN-related condition +1 more	GConflicting classifications of pathogenicity
Select item 189433	NM_001126049.2(KLLN):c.-794_-783del	KLLN, PTEN	Deletion (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
Select item 1746231	NM_001126049.2(KLLN):c.-785T>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488900	NM_001126049.2(KLLN):c.-790G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 142982	NM_001126049.2(KLLN):c.-797TGC[1]	KLLN, PTEN	Microsatellite (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 127663	NM_001126049.2(KLLN):c.-792C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GUncertain significance FDA Recognized database
Select item 1192233	NM_001126049.2(KLLN):c.-801C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 818504	NM_001126049.2(KLLN):c.-817_-801del	KLLN, PTEN	Deletion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488716	NM_001126049.2(KLLN):c.-801C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 503748	NM_001126049.2(KLLN):c.-804_-803delinsAA	KLLN, PTEN	Indel (5 prime UTR variant)	not provided	GUncertain significance
Select item 142652	NM_001126049.2(KLLN):c.-803T>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GUncertain significance
Select item 142844	NM_001126049.2(KLLN):c.-806A>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Cowden syndrome 1 +6 more	GConflicting classifications of pathogenicity
Select item 1337509	NM_001126049.2(KLLN):c.-808G>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 488939	NM_001126049.2(KLLN):c.-808G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 488866	NM_001126049.2(KLLN):c.-809T>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1739946	NM_001126049.2(KLLN):c.-810C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488786	NM_001126049.2(KLLN):c.-810C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GUncertain significance
Select item 141170	NM_001126049.2(KLLN):c.-810C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 140783	NM_001126049.2(KLLN):c.-812G>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GUncertain significance FDA Recognized database
Select item 127662	NM_001126049.2(KLLN):c.-812G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
Select item 3046566	NM_001126049.2(KLLN):c.-814C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN-related condition	GLikely benign
Select item 1738801	NM_001126049.2(KLLN):c.-814C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818474	NM_001126049.2(KLLN):c.-814C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822264	NM_001126049.2(KLLN):c.-817C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1736972	NM_001126049.2(KLLN):c.-821C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818444	NM_001126049.2(KLLN):c.-822_-821delinsTT	KLLN, PTEN	Indel (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1736658	NM_001126049.2(KLLN):c.-822C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1734982	NM_001126049.2(KLLN):c.-828C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 187362	NM_001126049.2(KLLN):c.-828C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Glioma susceptibility 2 +8 more	GUncertain significance
Select item 488717	NM_001126049.2(KLLN):c.-829C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1734359	NM_001126049.2(KLLN):c.-830G>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818430	NM_001126049.2(KLLN):c.-830G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818427	NM_001126049.2(KLLN):c.-831G>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818426	NM_001126049.2(KLLN):c.-831G>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2683786	NM_001126049.2(KLLN):c.-832G>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 822248	NM_001126049.2(KLLN):c.-837T>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 187000	NM_001126049.2(KLLN):c.-837T>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 234900	NM_001126049.2(KLLN):c.-838T>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488748	NM_001126049.2(KLLN):c.-839C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 234867	NM_001126049.2(KLLN):c.-840G>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 234632	NM_001126049.2(KLLN):c.-841_-840del	KLLN, PTEN	Deletion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 127661	NM_001126049.2(KLLN):c.-840G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
Select item 822240	NM_001126049.2(KLLN):c.-841G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488755	NM_001126049.2(KLLN):c.-844T>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1730126	NM_001126049.2(KLLN):c.-845C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141864	NM_001126049.2(KLLN):c.-845C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +6 more	GUncertain significance
Select item 488938	NM_001126049.2(KLLN):c.-846C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 189434	NM_001126049.2(KLLN):c.-848_-847insA	KLLN, PTEN	Insertion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 142892	NM_001126049.2(KLLN):c.-849C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 503509	NM_001126049.2(KLLN):c.-852T>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 1799026	NM_001126049.2(KLLN):c.-857C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1799011	NM_001126049.2(KLLN):c.-857C>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1799002	NM_001126049.2(KLLN):c.-857C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798680	NM_001126049.2(KLLN):c.-857del	KLLN, PTEN	Deletion (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798720	NM_001126049.2(KLLN):c.-858C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 488922	NM_001126049.2(KLLN):c.-860G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 234686	NM_001126049.2(KLLN):c.-861T>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 503505	NM_001126049.2(KLLN):c.-862A>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 503511	NM_001126049.2(KLLN):c.-870T>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488930	NM_001126049.2(KLLN):c.-873C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 822191	NM_001126049.2(KLLN):c.-874G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818366	NM_001126049.2(KLLN):c.-879C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 993234	NM_001126049.2(KLLN):c.-881G>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488885	NM_001126049.2(KLLN):c.-882A>C	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 488791	NM_001126049.2(KLLN):c.-882A>G	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 418430	NM_001126049.2(KLLN):c.-884C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 822160	NM_001126049.2(KLLN):c.-885C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822158	NM_001126049.2(KLLN):c.-886C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 189470	NM_001126049.2(KLLN):c.-886C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 548816	NM_001126049.2(KLLN):c.-887C>T	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	Cowden syndrome 1	GUncertain significance
Select item 189471	NM_001126049.2(KLLN):c.-887C>A	KLLN, PTEN	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 189435	NM_001126049.2(KLLN):c.-914_-889del	LOC130004273, KLLN +1 more	Deletion (5 prime UTR variant)	PTEN-related condition +2 more	GConflicting classifications of pathogenicity
Select item 224942	NM_001126049.2(KLLN):c.-897A>G	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GBenign
Select item 488788	NM_001126049.2(KLLN):c.-898G>C	LOC130004273, KLLN +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 127660	NM_001126049.2(KLLN):c.-898G>A	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
Select item 488921	NM_001126049.2(KLLN):c.-899C>A	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GUncertain significance
Select item 142058	NM_001126049.2(KLLN):c.-899C>G	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 818337	NM_001126049.2(KLLN):c.-902G>C	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141604	NM_001126049.2(KLLN):c.-902G>A	KLLN, LOC130004273 +1 more	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance

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