ces2[All Fields] AND 1[has_clinical] - dbVar

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nsv3902887

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48466242

variant

nsv3907590

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48470945

variant

nsv3897687

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48461042

variant

nsv3891351

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48454706

variant

nsv3894158

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48457513

variant

nsv3909307

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48472662

variant

nsv3900898

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 48464253

variant

nsv4455622

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1

Location information:

Clinical significance:

ID:: 49621257

variant

nsv3895916

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1; CES1P1

Location information:

Clinical significance:

ID:: 48459271

variant

10.

nsv3893460

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1P1; CES1

Location information:

Clinical significance:

ID:: 48456815

variant

11.

nsv3891816

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1; CES1P1

Location information:

Clinical significance:

ID:: 48455171

variant

12.

nsv3890958

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC107984881; CES2; CES4A; CES3

Location information:

Clinical significance:

ID:: 48454313

variant

13.

nsv4457115

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1P1; CES1P2; CES1

Location information:

Clinical significance:

ID:: 49622750

variant

14.

nsv3918978

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RN7SL543P; CES4A; CES3; LOC107984881; CES2

Location information:

Clinical significance:

ID:: 48482333

variant

15.

nsv3916542

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CES1; SNORA46; CDH8; MT1G; SETD6; SLC12A3; CES5A; SLC38A7; TIPINP2; MT1JP; CCDC102A; MTCH2P3; PLLP; MT1X; SPMIP8; MIR6772; OGFOD1; MT1M; LOC102725116; RN7SL645P; LOC105371296; LPCAT2; LOC105371293; CSNK2A2; MT2A; MMP2; LOC107984812; CAPNS2; CPNE2; LOC107984815; USB1; GNPATP; CNOT1; LOC388282; GINS3; LOC107984889; RPS27P27; MMP15; LOC105371287; CIAPIN1; LOC101927605; MT1B; MT1E; TRL-CAG2-2; RPS15AP34; BBS2; POLR2C; CCDC113; APOOP5; MT1H; LOC107984852; NUDT21; RNY5P9; RNU6-269P; DPPA2P4; LOC105371307; MT1IP; DUXAP11; RPS27AP16; LOC105371291; MT1F; LOC105371308; LINC02165; TRL-CAG2-1; MT1CP; MIR6863; RNU6-21P; GNAO1-AS1; LOC100421258; CES1P1; LOC107984867; CFAP20; LINC02141; ADGRG3; RN7SKP76; COQ9; LOC107984824; HMGB3P32; KIFC3; RNU6-1155P; NDRG4; HERPUD1; MMP2-AS1; LOC105371299; PRSS54; PSME3IP1; LOC105371302; MIR3935; RPL12P36; CCL22; MIR138-2; LOC105371300; CFAP69P1; AMFR; LOC112268167; KATNB1; GNAO1-DT; SLC6A2; MT1A; GOT2; ADGRG5; LOC105371280; NPAP1L; LOC105371283; RNU6-1110P; LOC105371306; NUP93-DT; UBE2FP2; CCL17; RNU6-103P; CETP; RPS24P17; MT4; MT1DP; ADGRG1; MT1L; RNU4-58P; ZNF319; RSPRY1; RNU6-20P; DRC7; NLRC5; GEMIN8P2; NUP93; DOK4; CNGB1; SNORA50A; LOC102723560; RPL23AP91; LOC105371298; LOC105371281; CES1P2; LOC105371301; CX3CL1; LOC101927536; GNAO1; LINC02137; MT3; RN7SL143P; LOC101927556; ARL2BP; See more...

Location information:

Clinical significance:

ID:: 48479897

variant

16.

nsv3916762

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RANBP10; TMEM208; CTCF-DT; RNU6-21P; GFOD2; LOC105371311; TPPP3; LOC105371308; PLEKHG4; LOC102723560; DYNC1LI2-DT; LOC100505942; CDH5; LOC107984894; ENKD1; CTCF; CDH16; TRADD; KCTD19; NAE1; LOC105371306; CMTM1; LOC105371309; SLC9A5; C16orf86; LINC02126; PARD6A; FHOD1; RN7SKP118; ZDHHC1; HSD11B2; RNA5SP428; CES2; LOC105371307; ATP6V0D1-DT; ACD; LOC105371310; FBXL8; E2F4; ELMO3; LINC00920; LOC105371318; CKLF-CMTM1; CMTM3; CES3; PHAF1; HSF4; RRAD; LOC729217; CES4A; MATCAP1; RN7SL543P; LOC107984823; CDH11; RPS15AP34; CA7; BEAN1; LOC107984821; DYNC1LI2; CIAO2B; PPIAP48; EXOC3L1; BEAN1-AS1; CKLF; LRRC36; LOC107984807; LINC02165; MIR328; ATP6V0D1; LOC107984881; TK2; NOL3; CMTM2; LOC105371313; RIPOR1; LOC105371316; PDP2; FBXL9P; CBFB; AGRP; LOC107984822; B3GNT9; LINC00922; CMTM4; RNU1-123P; CARMIL2; UBE2FP2; TERB1; LOC105371317; See more...

Location information:

Clinical significance:

ID:: 48480117

variant

17.

nsv4675201

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC100420066; LINC00920; VPS4A; ESRP2; LOC105371321; CYB5B; RNU4-30P; LOC107984823; UTP4; PDF; CDH5; CTCF; HSF4; ENKD1; ZFP90; SNTB2; KCTD19; RNU6-898P; TRADD; NIP7; TERF2; RPS12P27; RNU1-123P; DUS2; CMTM1; HAS3; LCAT; KARS1P3; NAE1; DPEP3; SLC9A5; SNORD13H; PLA2G15; PDPR; C16orf86; LOC105371317; CENPT; PRMT7; CBFB; CDH16; AGRP; RNU4-36P; MIR1972-2; B3GNT9; NONOP1; DERPC; PDXDC2P-NPIPB14P; RPS2P45; PDXDC2P; RNU6-1262P; LOC101060098; TERB1; RNU6-359P; PARD6A; DPEP2; FHOD1; CARMIL2; NFATC3; RN7SKP118; SMPD3; SLC7A6; CTRL; TSNAXIP1; LOC105371325; TMEM208; MIR140; RANBP10; CMTM4; PLEKHG4; LOC107984807; THAP11; EDC4; MIR6773; CIAO2B; CTCF-DT; PSMB10; GFOD2; DYNC1LI2; ATP6V0D1; TPPP3; LOC100418868; CKLF; DPEP2NB; CDH1; COG8; RNU6-22P; MIR328; RNA5SP428; LRRC36; NRN1L; NUTF2; FBXL9P; CLEC18A; TK2; WWP2; TANGO6; RIPOR1; HSPE1P5; ATP6V0D1-DT; FTLP14; MIR1538; NPIPB14P; DDX28; EXOC3L1; LOC107984881; NFAT5; BEAN1-AS1; LOC100421641; NOL3; CHTF8; ZDHHC1; HSD11B2; CMTM2; LOC107984821; ACD; CES2; PDP2; RPL35AP33; ELMO3; CDH3; E2F4; PSKH1; LOC105371316; SLC12A4; SLC7A6OS; PHAF1; NOB1; RPS10P24; NQO1; FBXL8; CES4A; CKLF-CMTM1; RN7SL543P; CA7; RNU7-42P; RNA5SP429; BEAN1; LOC105371318; CMTM3; DYNC1LI2-DT; LOC100505942; RRAD; MATCAP1; CES3; TMED6; See more...

Location information:

Clinical significance:

ID:: 50272026

variant

18.

nsv6315060

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105371283; MT1A; LOC105371280; CCL17; MTND5P34; SLC6A2; NUP93-DT; PLLP; MIR138-2; GNAO1-DT; MT1G; CCL22; AMFR; RPL31P56; ADGRG1; RSPRY1; LOC105371277; RN7SL841P; MT1DP; ADGRG5; RPL23AP91; RPS24P17; LOC105371274; FTO-IT1; MT4; IRX6; CFAP69P1; LINC02140; CETP; DOK4; CES1P1; MIR6863; GNAO1-AS1; MT1L; MT1CP; IRX5; LOC105371271; LOC105371291; MT1F; MMP2-AS1; PSME3IP1; LOC105371279; HMGB3P32; MIR3935; HERPUD1; LOC101927480; TRL-CAG2-1; COQ9; CRNDE; MMP2; MT2A; LPCAT2; LOC105371276; OGFOD1; CAPNS2; LOC107984815; LINC02183; MT1M; CPNE2; LINC02169; MT1IP; POLR2C; BBS2; DPPA2P4; MT1H; CIAPIN1; NUDT21; MT1E; LOC105371287; LOC107984889; TRL-CAG2-2; MT1B; LOC101927536; MT3; LOC105371278; LOC102725116; LOC105371275; ARL2BP; LOC105371281; FTO; NUP93; CX3CL1; CCDC102A; IRX3; CES1P2; LOC105371272; CES5A; MT1X; SLC12A3; GNAO1; NLRC5; CES1; MT1JP; See more...

Location information:

Clinical significance:

ID:: 53679466

variant

19.

nsv3910745

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PSMB10; TPPP3; ATP6V0D1; GFOD2; CKLF; CIAO2B; TSNAXIP1; NRN1L; LOC107984807; CMTM3; PHAF1; LINC00920; ZDHHC1; ATP6V0D1-DT; PSKH1; RRAD; CES3; CA7; LOC107984823; PDP2; CES2; HSD11B2; NOL3; ACD; NUTF2; RNA5SP428; DDX28; SLC12A4; LOC105371313; FBXL8; ELMO3; E2F4; LOC105371310; LCAT; DPEP3; DYNC1LI2-DT; CMTM1; DUS2; TRADD; LOC107984894; LINC02126; C16orf86; CDH5; RNU6-359P; CKLF-CMTM1; LOC105371318; SLC9A5; RN7SL543P; CDH11; CTCF; MATCAP1; ENKD1; LOC100505942; HSF4; PPIAP48; BEAN1; CES4A; CTCF-DT; CTRL; KARS1P3; RANBP10; TMEM208; DPEP2NB; LOC107984822; PLEKHG4; CMTM4; THAP11; EDC4; LOC105371317; LOC105371311; CENPT; B3GNT9; CARMIL2; LINC00922; AGRP; CBFB; RN7SKP118; KCTD19; FHOD1; PARD6A; RNU1-123P; DPEP2; NAE1; CDH16; DYNC1LI2; LOC107984881; LRRC36; TERB1; TK2; LOC107984821; MIR328; LOC105371316; EXOC3L1; CMTM2; RIPOR1; BEAN1-AS1; FBXL9P; See more...

Location information:

Clinical significance:

ID:: 48474100

variant

20.

nsv7094682

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RNA5SP428; PHAF1; CA7; CES3; FBXL8; CES2; LOC105371316; DYNC1LI2-DT; CMTM3; MATCAP1; RRAD; CES4A; HSF4; BEAN1; LOC105371318; RN7SL543P; CKLF-CMTM1; LOC107984823; CDH5; CDH16; CBFB; NAE1; CMTM1; TRADD; LOC105371317; B3GNT9; CMTM4; TERB1; LOC107984881; LOC107984821; BEAN1-AS1; CKLF; LOC107984807; CIAO2B; DYNC1LI2; PDP2; CMTM2; TK2; NOL3; LINC00920; See more...

Location information:

Clinical significance:

ID:: 55274871

variant

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