cdipt[All Fields] AND 1[has_clinical] - dbVar - NCBI

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1.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MVP; CDIPT; SEZ6L2; PAGR1; PRRT2; KCTD13; ASPHD1; CDIPTOSP

Location information:

Clinical significance:

ID:: 48441701

variant

2.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC107984874; RRN3P2; INO80E; TMEM219; SLX1A; RNU6-1005P; LOC105371143; ABCA3P1; SDR42E2; LOC613038; ZG16; TPRKBP2; LOC107984851; DOC2A; HS3ST4; GTF3C1; KATNIP; SNX29P2; SLC5A11; TAOK2; TBX6; ERN2; IL21R; EIF3C; LINC02191; NSMCE1; LOC105371126; GAPDHP35; LOC112268176; CORO1A-AS1; SLC7A5P1; LOC554206; LOC100421169; LOC100421173; RNU6-159P; SEZ6L2; RNU6-196P; EEF2K; SULT1A4; KDM8; LINC02194; ALDOA; RNU7-24P; RABEP2; PALB2; CYCSP39; NPIPB13; QPRT; SMG1P5; SMG1P2; EEF1A1P38; CDR2; UQCRC2; LOC105371159; SMG1P1; USP31; LOC112268175; UBFD1; NDUFAB1; SCML2P2; PLK1; RNY1P10; NPIPB9; CCNYL7; RNA5SP405; PRKCB; GDPD3; ARHGAP17; HIRIP3; HSPE1P16; IL27; SLX1B-SULT1A4; ATP2A1; BOLA2B; TBC1D10B; VWA3A; LINC02175; EIF3CL; POLR3E; BOLA2; LOC105371131; HS3ST2; EARS2; OTOA; CACNG3; CDC37P1; KCTD13; LOC105371168; HMGN2P3; KCTD13-DT; IL4R; ZKSCAN2; SBK1; TNRC6A; DCTN5; ATP2A1-AS1; SLX1A-SULT1A3; LOC100128079; CDIPTOSP; RN7SKP23; LOC101928215; LOC100129184; MIR4721; MIR548W; LOC102723536; GGA2; TLCD3B; LOC105371147; TRL-TAG3-1; LOC100421031; LOC105371150; MIR3680-2; IGSF6; SULT1A3; KIF22; LOC107984835; SEPTIN1; LOC105371167; CA5AP1; LOC102723708; RPS15AP33; MIR6862-2; RRN3P3; BOLA2-SMG1P6; MAZ; XPO6; LOC105371153; CD19; C16orf82; AQP8; MOSMO; ASPHD1; MYL11; SMG1P4; PAGR1; LINC01567; SGF29; SCNN1G; NPIPB8; MFSD13B; NPIPB4; LCMT1; SULT1A1; NPIPB5; MVP; MIR4517; NPIPB10P; LOC100420536; COG7; YPEL3-DT; LAT; LOC112694756; SLX1B; LOC105369297; PAWRP2; IL21R-AS1; LOC105371129; LOC100420641; NPIPB7; LOC606724; LOC105371155; C16orf54; LINC02195; CLN3; LOC105371149; RBBP6; LOC112268174; PRRT2; LOC101927814; NPIPB12; SH2B1; PDZD9; CD2BP2-DT; MIR6862-1; RN7SL557P; OTOAP1; CORO1A; LOC100420644; MAPK3; APOBR; LOC107984829; LCMT1-AS2; MIR1273H; METTL9; NPIPB11; LOC100421171; TUFM; CD2BP2; SPN; SULT1A2; RNU6-1241P; C16orf92; MVP-DT; SCNN1B; RRN3P1; TRL-AAG2-4; NUPR1; LOC105371157; LCMT1-AS1; LOC105371154; NSMCE1-DT; LOC388242; ATXN2L; SMG1P6; CDIPT; CHP2; PPP4C; RN7SKP127; GSG1L; YPEL3; CDC37P2; SPNS1; NFATC2IP; LOC101929894; ZNF48; SUB1P4; CDR2-DT; LOC101928188; NPIPB6; See more...

Location information:

Clinical significance:

ID:: 48469210

variant

3.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SPN; LOC101928188; NFATC2IP; SPNS1; LOC101929894; MVP-DT; SULT1A2; SMG1P6; GDPD3; NPIPB9; CDC37P2; BOLA2B; CDC37P1; PPP4C; ATXN2L; RN7SKP127; NPIPB10P; SH2B1; SULT1A1; C16orf54; CLN3; CORO1A; NPIPB7; MAPK3; NPIPB11; APOBR; PRRT2; YPEL3-DT; SLX1B; LOC112694756; PAWRP2; CORO1A-AS1; SLX1A; MIR4517; EIF3C; LAT; LOC606724; PAGR1; SULT1A3; SGF29; RPS15AP33; MVP; ASPHD1; MIR6862-2; LOC102723708; NPIPB8; NPIPB12; LOC100129184; MAZ; TUFM; MIR4721; ATP2A1-AS1; LOC107984835; LOC105371167; TLCD3B; LOC388242; MIR3680-2; NUPR1; CDIPTOSP; KIF22; SLX1A-SULT1A3; HIRIP3; KCTD13-DT; SULT1A4; LOC105371168; LOC101928215; RABEP2; KCTD13; SMG1P2; IL27; EIF3CL; BOLA2; NPIPB13; SLX1B-SULT1A4; SMG1P5; ATP2A1; CD19; ALDOA; QPRT; BOLA2-SMG1P6; CA5AP1; LOC105371159; TBX6; SNX29P2; RRN3P2; SLC7A5P1; ZG16; TAOK2; SEZ6L2; YPEL3; DOC2A; CDIPT; INO80E; LOC613038; C16orf92; TMEM219; See more...

Location information:

Clinical significance:

ID:: 48477057

variant

4.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CA5AP1; NPIPB13; LOC105371159; CD19; SGF29; ALDOA; MVP; PAGR1; BOLA2-SMG1P6; SULT1A3; MAZ; CDIPTOSP; NPIPB8; MIR6862-2; LOC102723708; RPS15AP33; ASPHD1; LOC105371167; LOC100129184; LOC107984835; KIF22; MIR4721; ATP2A1-AS1; LOC101928215; MAPK3; SLX1A-SULT1A3; NPIPB7; NPIPB12; SH2B1; TUFM; TLCD3B; MIR3680-2; C16orf54; LOC388242; NPIPB11; NUPR1; CORO1A; PRRT2; LOC606724; SLX1B; PAWRP2; NPIPB10P; SULT1A1; CLN3; TBX6; APOBR; LAT; YPEL3-DT; LOC112694756; SLC7A5P1; EIF3C; MIR4517; ZG16; CORO1A-AS1; CDIPT; SLX1A; LOC101929894; RN7SKP127; SPNS1; ATXN2L; PPP4C; RRN3P2; SULT1A2; LOC101928188; SNX29P2; DOC2A; NFATC2IP; TAOK2; LOC613038; INO80E; YPEL3; BOLA2B; SEZ6L2; TMEM219; C16orf92; SPN; MVP-DT; KCTD13-DT; NPIPB9; HIRIP3; ATP2A1; GDPD3; KCTD13; SMG1P6; CDC37P1; BOLA2; SLX1B-SULT1A4; SMG1P5; RABEP2; SULT1A4; LOC105371168; QPRT; IL27; SMG1P2; See more...

Location information:

Clinical significance:

ID:: 54356329

variant

5.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SULT1A1; CLN3; PRRT2; NPIPB10P; SLX1B; CORO1A; NPIPB11; LOC606724; MAPK3; APOBR; CD19; ALDOA; SULT1A3; PAGR1; SGF29; NPIPB13; CA5AP1; MVP; LOC105371159; BOLA2-SMG1P6; ASPHD1; MIR4721; RPS15AP33; LOC107984835; LOC100129184; NPIPB8; LOC102723708; MIR6862-2; MAZ; KIF22; ATP2A1-AS1; HIRIP3; GDPD3; NPIPB9; NFATC2IP; SPNS1; SPN; SULT1A2; SMG1P6; BOLA2B; ATXN2L; RN7SKP127; ATP2A1; CDC37P1; IL27; LOC105371168; RABEP2; QPRT; SMG1P5; SULT1A4; BOLA2; SLX1B-SULT1A4; SMG1P2; KCTD13-DT; KCTD13; SLC7A5P1; PAWRP2; YPEL3-DT; CORO1A-AS1; LAT; SLX1A; LOC112694756; EIF3C; RRN3P2; MIR4517; SNX29P2; TMEM219; LOC101928188; LOC101929894; TBX6; INO80E; CDIPT; DOC2A; MVP-DT; TAOK2; SEZ6L2; C16orf92; TUFM; MIR3680-2; ZG16; LOC613038; LOC105371167; C16orf54; PPP4C; TLCD3B; SH2B1; YPEL3; NPIPB12; NPIPB7; LOC388242; NUPR1; CDIPTOSP; SLX1A-SULT1A3; LOC101928215; See more...

Location information:

Clinical significance:

ID:: 48478480

variant

6.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: MIR4517; PAWRP2; SLC7A5P1; CORO1A-AS1; EIF3C; LAT; LOC112694756; YPEL3-DT; LOC101928188; TMEM219; INO80E; SNX29P2; RRN3P2; C16orf92; ZG16; MVP-DT; DOC2A; YPEL3; SEZ6L2; TAOK2; TBX6; PPP4C; CDIPT; SULT1A2; SPNS1; SMG1P6; SPN; HIRIP3; GDPD3; NPIPB9; CDC37P1; ATP2A1; ATXN2L; RN7SKP127; NFATC2IP; CDC37P2; KCTD13-DT; QPRT; SULT1A4; LOC105371168; RABEP2; KCTD13; SLX1B-SULT1A4; BOLA2; EIF3CL; SMG1P2; IL27; ALDOA; CD19; MVP; CA5AP1; BOLA2-SMG1P6; LOC100129184; LOC105371159; ASPHD1; PAGR1; SGF29; MAZ; MIR4721; KIF22; MIR6862-2; ATP2A1-AS1; NPIPB8; RPS15AP33; LOC102723708; LOC107984835; MIR3680-2; C16orf54; TLCD3B; LOC105371167; SH2B1; TUFM; NPIPB12; LOC101928215; LOC388242; NUPR1; NPIPB7; NPIPB10P; NPIPB11; CLN3; SULT1A1; CDIPTOSP; APOBR; PRRT2; CORO1A; LOC606724; MAPK3; SLX1B; See more...

Location information:

Clinical significance:

ID:: 48487944

variant

7.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TBX6; LAT; EIF3C; ZG16; KCTD13-DT; MIR4517; SLC7A5P1; LOC100129184; LOC105371168; NPIPB8; ATP2A1-AS1; CDIPTOSP; KIF22; MIR4721; MAZ; ASPHD1; RPS15AP33; SH2B1; NPIPB12; NPIPB7; MAPK3; LOC105371159; BOLA2-SMG1P6; LOC388242; CORO1A; NUPR1; NPIPB11; TLCD3B; TUFM; C16orf54; MIR3680-2; SMG1P2; SULT1A4; IL27; LOC105371167; BOLA2; EIF3CL; MIR6862-2; SLX1B-SULT1A4; LOC102723708; LOC107984835; CD19; QPRT; RABEP2; ALDOA; LOC101928215; MVP; CA5AP1; SGF29; NFATC2IP; INO80E; PPP4C; ATXN2L; YPEL3; PAGR1; SPNS1; TMEM219; SNX29P2; SULT1A2; DOC2A; TAOK2; C16orf92; RRN3P2; CDIPT; GDPD3; SMG1P6; SEZ6L2; CORO1A-AS1; SPN; ATP2A1; LOC112694756; CDC37P2; CDC37P1; HIRIP3; KCTD13; NPIPB10P; SLX1B; NPIPB9; PRRT2; YPEL3-DT; LOC606724; MVP-DT; SULT1A1; LOC101928188; PAWRP2; RN7SKP127; APOBR; CLN3; See more...

Location information:

Clinical significance:

ID:: 48484306

variant

8.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC102723708; MAZ; LOC100129184; ATP2A1-AS1; MIR6862-2; NPIPB8; MIR4721; PAGR1; RPS15AP33; KIF22; ASPHD1; LAT; SGF29; YPEL3-DT; LOC112694756; PAWRP2; MIR4517; SLC7A5P1; APOBR; EIF3C; MAPK3; LOC606724; PRRT2; SLX1B; NPIPB10P; NPIPB7; SULT1A1; CLN3; NPIPB11; SMG1P6; SPNS1; RN7SKP127; ATXN2L; SULT1A2; SPN; NFATC2IP; ATP2A1; NPIPB9; HIRIP3; GDPD3; CDC37P1; DOC2A; PPP4C; CDIPT; TMEM219; SNX29P2; TBX6; LOC101928188; C16orf92; RRN3P2; MVP-DT; TAOK2; INO80E; YPEL3; ZG16; LOC105371159; SEZ6L2; ALDOA; CA5AP1; CD19; BOLA2-SMG1P6; MVP; BOLA2; SMG1P2; IL27; KCTD13-DT; LOC105371168; SLX1B-SULT1A4; KCTD13; RABEP2; QPRT; SULT1A4; LOC101928215; NPIPB12; CDIPTOSP; SH2B1; LOC107984835; C16orf54; NUPR1; TLCD3B; LOC388242; LOC105371167; MIR3680-2; TUFM; See more...

Location information:

Clinical significance:

ID:: 48470987

variant

9.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: BOLA2; SLX1B-SULT1A4; SULT1A4; QPRT; SMG1P2; RABEP2; LOC105371168; MAPK3; SH2B1; NPIPB12; LOC101928215; TUFM; MIR3680-2; NPIPB7; TLCD3B; C16orf54; NPIPB11; NUPR1; LOC388242; LOC102723708; NPIPB8; MAZ; MIR6862-2; CDIPTOSP; LOC100129184; LOC107984835; LOC105371167; ASPHD1; MIR4721; RPS15AP33; ATP2A1-AS1; KIF22; LAT; YPEL3-DT; INO80E; TBX6; LOC112694756; EIF3C; SLC7A5P1; ZG16; APOBR; PRRT2; LOC606724; PAWRP2; NPIPB10P; CLN3; SLX1B; SULT1A1; IL27; MIR4517; ATP2A1; SMG1P6; HIRIP3; NPIPB9; SPN; GDPD3; KCTD13; RN7SKP127; CDIPT; KCTD13-DT; DOC2A; CDC37P1; SNX29P2; SPNS1; SULT1A2; PPP4C; TMEM219; SEZ6L2; C16orf92; TAOK2; RRN3P2; ATXN2L; NFATC2IP; MVP-DT; LOC101928188; CA5AP1; YPEL3; SGF29; PAGR1; BOLA2-SMG1P6; MVP; LOC105371159; CD19; ALDOA; See more...

Location information:

Clinical significance:

ID:: 49621544

variant

10.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: ATP2A1; IL27; RN7SKP127; KCTD13; SMG1P6; MVP-DT; SPN; CDC37P1; GDPD3; LOC101928188; HIRIP3; SMG1P2; BOLA2; BOLA2-SMG1P6; LOC105371159; SULT1A4; QPRT; RABEP2; CD19; CA5AP1; SLX1B-SULT1A4; PAGR1; SGF29; MVP; ALDOA; CDIPTOSP; LOC101928215; MAZ; NPIPB8; KIF22; ASPHD1; NPIPB12; MIR3680-2; LOC100129184; LOC102723708; MIR6862-2; SH2B1; ATP2A1-AS1; MAPK3; TUFM; NPIPB11; TLCD3B; NUPR1; MIR4721; LOC388242; NPIPB7; NPIPB10P; LOC105371167; PRRT2; YPEL3-DT; RPS15AP33; LOC107984835; C16orf54; SLX1B; LOC112694756; LOC606724; SULT1A1; APOBR; CLN3; TBX6; LAT; MIR4517; INO80E; ZG16; PAWRP2; EIF3C; TAOK2; ATXN2L; SLC7A5P1; NFATC2IP; SNX29P2; CDIPT; PPP4C; SEZ6L2; YPEL3; SULT1A2; SPNS1; C16orf92; TMEM219; KCTD13-DT; DOC2A; NPIPB9; RRN3P2; LOC105371168; See more...

Location information:

Clinical significance:

ID:: 50271738

variant

11.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SMG1P2; SULT1A4; ALDOA; RABEP2; QPRT; LOC105371159; PRRT2; C16orf54; SH2B1; LOC388242; NPIPB12; TUFM; NPIPB7; NUPR1; NPIPB11; MAPK3; CLN3; CDIPTOSP; LOC101928215; LOC100129184; TLCD3B; KIF22; LOC107984835; RPS15AP33; MIR3680-2; MIR4721; LOC105371167; MAZ; ATP2A1-AS1; NPIPB8; TBX6; LOC112694756; RRN3P2; INO80E; SNX29P2; TMEM219; SLC7A5P1; ZG16; DOC2A; EIF3C; NPIPB10P; TAOK2; SEZ6L2; SLX1B; YPEL3-DT; SULT1A1; MIR4517; PAWRP2; ATP2A1; LAT; LOC606724; APOBR; GDPD3; HIRIP3; IL27; KCTD13-DT; CDC37P1; LOC105371168; PPP4C; ATXN2L; KCTD13; NPIPB9; CDIPT; SMG1P6; SLX1B-SULT1A4; BOLA2; NFATC2IP; LOC101928188; SPNS1; C16orf92; RN7SKP127; YPEL3; SULT1A2; SPN; CA5AP1; MVP-DT; LOC102723708; CD19; SGF29; ASPHD1; MIR6862-2; PAGR1; MVP; BOLA2-SMG1P6; See more...

Location information:

Clinical significance:

ID:: 49621316

variant

12.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TAOK2; ZG16; DOC2A; SLC7A5P1; SEZ6L2; RRN3P2; YPEL3; TMEM219; CORO1A-AS1; INO80E; SNX29P2; TBX6; CDIPT; SULT1A2; MVP-DT; CDC37P1; C16orf92; GDPD3; SMG1P6; NFATC2IP; SPNS1; SPN; LOC101928188; ATXN2L; RN7SKP127; PPP4C; KCTD13; HIRIP3; RABEP2; LOC105371168; NPIPB9; IL27; KCTD13-DT; SLX1B-SULT1A4; BOLA2; SULT1A4; ATP2A1; BOLA2-SMG1P6; QPRT; SMG1P2; ALDOA; CA5AP1; LOC105371159; PAGR1; ASPHD1; MVP; SGF29; RPS15AP33; MIR6862-2; MAZ; LOC102723708; CD19; ATP2A1-AS1; KIF22; TLCD3B; NPIPB8; TUFM; NUPR1; MIR4721; LOC100129184; LOC105371167; NPIPB12; MIR3680-2; LOC388242; LOC101928215; LOC107984835; NPIPB11; APOBR; CORO1A; CDIPTOSP; CLN3; NPIPB10P; SH2B1; PRRT2; MAPK3; MIR4517; C16orf54; SULT1A1; YPEL3-DT; LOC112694756; PAWRP2; SLX1B; LAT; EIF3C; LOC606724; See more...

Location information:

Clinical significance:

ID:: 48461456

variant

13.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TMEM219; SPNS1; LOC101928188; SULT1A2; SMG1P6; NFATC2IP; C16orf92; SPN; CDIPT; MVP-DT; ATXN2L; RN7SKP127; SEZ6L2; DOC2A; MIR3680-2; YPEL3; PPP4C; CLN3; TUFM; NUPR1; LOC388242; NPIPB11; NPIPB12; C16orf54; SH2B1; PRRT2; MAPK3; CORO1A; MIR4517; SULT1A1; PAWRP2; NPIPB10P; SLX1B; YPEL3-DT; LAT; LOC606724; APOBR; PAGR1; SGF29; BOLA2-SMG1P6; CD19; CA5AP1; MVP; MIR6862-2; KIF22; RPS15AP33; MIR4721; LOC107984835; ASPHD1; LOC105371167; LOC100129184; TLCD3B; CDIPTOSP; LOC102723708; LOC101928215; NPIPB9; KCTD13; ATP2A1-AS1; NPIPB8; MAZ; LOC105371168; CDC37P1; GDPD3; KCTD13-DT; HIRIP3; SLX1B-SULT1A4; IL27; ATP2A1; QPRT; ALDOA; SULT1A4; LOC105371159; RABEP2; SLC7A5P1; BOLA2; SMG1P2; SNX29P2; RRN3P2; LOC112694756; TBX6; ZG16; EIF3C; TAOK2; CORO1A-AS1; INO80E; See more...

Location information:

Clinical significance:

ID:: 48478560

variant

14.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SEZ6L2; C16orf92; YPEL3; ZG16; RN7SKP127; CDIPT; TAOK2; MVP-DT; ATXN2L; DOC2A; SNX29P2; NFATC2IP; PPP4C; LOC101928188; INO80E; TMEM219; RRN3P2; SULT1A2; SPNS1; KCTD13; NPIPB9; CDC37P1; ATP2A1; HIRIP3; GDPD3; SMG1P6; SPN; RABEP2; QPRT; LOC105371168; IL27; SLX1B-SULT1A4; SMG1P2; BOLA2; SULT1A4; KCTD13-DT; SGF29; PAGR1; MVP; BOLA2-SMG1P6; LOC105371159; CA5AP1; ASPHD1; CD19; ALDOA; MIR4721; NPIPB8; RPS15AP33; KIF22; LOC105371167; ATP2A1-AS1; MAZ; MIR6862-2; LOC107984835; LOC102723708; NUPR1; LOC100129184; TLCD3B; MAPK3; LOC388242; MIR3680-2; SH2B1; TUFM; NPIPB12; NPIPB11; C16orf54; LOC101928215; CDIPTOSP; SULT1A1; PRRT2; SLX1B; LOC606724; CLN3; NPIPB10P; APOBR; MIR4517; SLC7A5P1; EIF3C; LAT; PAWRP2; LOC112694756; YPEL3-DT; TBX6; See more...

Location information:

Clinical significance:

ID:: 50373555

variant

15.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: KCTD13; SLX1B-SULT1A4; BOLA2; SMG1P2; ATP2A1; LOC105371168; RABEP2; QPRT; KCTD13-DT; BOLA2-SMG1P6; SULT1A4; CA5AP1; LOC105371159; CD19; ALDOA; MVP; SGF29; KIF22; ASPHD1; PAGR1; LOC102723708; MAZ; MIR6862-2; NPIPB8; LOC100129184; RPS15AP33; MIR4721; LOC388242; TUFM; TLCD3B; NUPR1; LOC101928215; SH2B1; ATP2A1-AS1; MIR3680-2; CDIPTOSP; LOC105371167; NPIPB12; C16orf54; LOC107984835; NPIPB11; CORO1A; MAPK3; NPIPB10P; PRRT2; SULT1A1; LOC606724; MIR4517; LAT; EIF3C; SLC7A5P1; LOC112694756; SLX1B; CORO1A-AS1; YPEL3-DT; MVP-DT; PAWRP2; YPEL3; SEZ6L2; PPP4C; CDIPT; SNX29P2; TAOK2; TBX6; TMEM219; INO80E; C16orf92; ZG16; LOC101928188; DOC2A; RRN3P2; CDC37P1; ATXN2L; NFATC2IP; RN7SKP127; SMG1P6; GDPD3; HIRIP3; SPN; SULT1A2; SPNS1; NPIPB9; See more...

Location information:

Clinical significance:

ID:: 48486775

variant

16.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC606724; YPEL3-DT; LOC112694756; SLX1B; SLC7A5P1; SEZ6L2; ZG16; DOC2A; TAOK2; YPEL3; TMEM219; RRN3P2; INO80E; SNX29P2; CORO1A-AS1; TBX6; CDIPT; PPP4C; MVP-DT; C16orf92; SPN; GDPD3; LOC101928188; SMG1P6; RN7SKP127; SLX1B-SULT1A4; BOLA2; KCTD13; HIRIP3; LOC105371168; KCTD13-DT; SULT1A4; LOC105371159; BOLA2-SMG1P6; QPRT; ALDOA; SMG1P2; LOC102723708; MAZ; CA5AP1; ASPHD1; PAGR1; MVP; LOC101928215; TLCD3B; KIF22; NPIPB12; MIR3680-2; LOC105371167; LOC100129184; CDIPTOSP; PRRT2; MAPK3; CORO1A; NPIPB10P; LOC388242; NPIPB11; C16orf54; See more...

Location information:

Clinical significance:

ID:: 49344536

variant

17.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PPP4C; MVP-DT; RN7SKP127; GDPD3; CDIPT; ZNF771; LOC101929894; SPN; C16orf92; MYL11; MAZ; CA5AP1; MVP; ZNF785; SULT1A3; MIR4518; PAGR1; RPL7L1P16; FBRS; ASPHD1; SMG1P2; SMG1P5; SEPHS2; NPIPB13; ZNF747; ALDOA; QPRT; CORO1A; PRR14; ITGAL; CD2BP2-DT; ZNF688; MAPK3; PRRT2; DCTPP1; C16orf54; CD2BP2; ZNF768; SNORA80C; RNU6-416P; SLX1A-SULT1A3; CDIPTOSP; SEPTIN1; LOC105371167; LOC100421031; ZNF747-DT; MIR3680-2; TLCD3B; TAOK2; DOC2A; KIF22; SEZ6L2; RNU7-61P; TBX6; ZG16; LOC613038; CORO1A-AS1; YPEL3; TMEM219; ZNF48; INO80E; SLX1A; SLC7A5P1; YPEL3-DT; LOC112694756; TBC1D10B; HIRIP3; ZNF764; LOC105371168; KCTD13; BOLA2B; KCTD13-DT; ZNF689; See more...

Location information:

Clinical significance:

ID:: 48475006

variant

18.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PAGR1; SULT1A3; CA5AP1; MVP; ALDOA; BOLA2-SMG1P6; LOC105371167; ASPHD1; KIF22; MAZ; CDIPTOSP; SLX1A-SULT1A3; TLCD3B; MIR3680-2; NPIPB11; LOC388242; CORO1A; MAPK3; C16orf54; NPIPB12; LOC606724; PRRT2; SLC7A5P1; SLX1B; CORO1A-AS1; TBX6; ZG16; YPEL3-DT; LOC112694756; SLX1A; INO80E; MVP-DT; DOC2A; SEZ6L2; CDIPT; TAOK2; C16orf92; RN7SKP127; SNX29P2; LOC101929894; YPEL3; TMEM219; PPP4C; LOC613038; KCTD13; BOLA2B; HIRIP3; SPN; QPRT; SMG1P6; LOC105371168; KCTD13-DT; GDPD3; SLX1B-SULT1A4; BOLA2; SMG1P2; NPIPB13; SMG1P5; SULT1A4; See more...

Location information:

Clinical significance:

ID:: 48458226

variant

19.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: BOLA2B; SPN; RN7SKP127; LOC101929894; PPP4C; SMG1P6; HIRIP3; GDPD3; KCTD13; SULT1A4; SLX1B-SULT1A4; SMG1P2; BOLA2; KCTD13-DT; LOC105371168; BOLA2-SMG1P6; CA5AP1; ALDOA; SMG1P5; NPIPB13; QPRT; MVP; MAZ; SULT1A3; ASPHD1; PAGR1; KIF22; SLX1A-SULT1A3; LOC388242; NPIPB12; CDIPTOSP; LOC105371167; TLCD3B; MIR3680-2; C16orf54; PRRT2; CORO1A; MAPK3; LOC606724; YPEL3-DT; LOC112694756; SLX1A; CORO1A-AS1; SLX1B; SEZ6L2; MVP-DT; CDIPT; YPEL3; TBX6; INO80E; LOC613038; TMEM219; C16orf92; TAOK2; ZG16; DOC2A; SLC7A5P1; See more...

Location information:

Clinical significance:

ID:: 48455824

variant

20.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SLX1B; LOC606724; LOC112694756; YPEL3-DT; SLC7A5P1; ZG16; DOC2A; TAOK2; YPEL3; LOC613038; SEZ6L2; CDIPT; TMEM219; INO80E; TBX6; SLX1A; CORO1A-AS1; C16orf92; MVP-DT; LOC101929894; RN7SKP127; BOLA2B; PPP4C; SPN; SMG1P6; GDPD3; LOC105371168; SLX1B-SULT1A4; KCTD13; BOLA2; HIRIP3; QPRT; SULT1A4; KCTD13-DT; BOLA2-SMG1P6; NPIPB13; ALDOA; PAGR1; SULT1A3; SMG1P2; MVP; ASPHD1; CA5AP1; MAZ; MIR3680-2; LOC105371167; CDIPTOSP; NPIPB12; KIF22; TLCD3B; SLX1A-SULT1A3; LOC388242; CORO1A; PRRT2; MAPK3; C16orf54; See more...

Location information:

Clinical significance:

ID:: 54356563

variant

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cdipt[All Fields] AND 1[has_clinical] (247)
dbVar
Mastomys coucha isolate ucsf_1 unplaced genomic scaffold, UCSF_Mcou_1 pScaffold2...
Mastomys coucha isolate ucsf_1 unplaced genomic scaffold, UCSF_Mcou_1 pScaffold22, whole genome shotgun sequence
gi|1767187803|gnl|ASM:GCF_008632905 caffold22|ref|NW_022196905.1||gpp|GPS_018968019.1|

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