iqsec3[All Fields] AND 1[has_clinical] - dbVar

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nsv3891216

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3

Location information:

Clinical significance:

ID:: 48454571

variant

nsv3890190

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3

Location information:

Clinical significance:

ID:: 48453545

variant

nsv3903348

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SLC6A12; IQSEC3-AS1

Location information:

Clinical significance:

ID:: 48466703

variant

nsv4684316

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3-AS2; IQSEC3

Location information:

Clinical significance:

ID:: 50287439

variant

nsv3910326

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3; LOC574538

Location information:

Clinical significance:

ID:: 48473681

variant

nsv3906668

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3-AS2; IQSEC3; LOC574538

Location information:

Clinical significance:

ID:: 48470023

variant

nsv3891219

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: IQSEC3-AS2; IQSEC3; LOC574538

Location information:

Clinical significance:

ID:: 48454574

variant

nsv3910307

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC574538; IQSEC3; IQSEC3-AS2

Location information:

Clinical significance:

ID:: 48473662

variant

nsv4455273

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC574538; SLC6A12; IQSEC3; IQSEC3-AS1

Location information:

Clinical significance:

ID:: 49620908

variant

10.

nsv4457052

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TSPAN9; RNU6-174P; GALNT8; RPS15P7; FGF6; THCAT155; TULP3; SLC6A12; LOC105369612; PARP11-AS1; LINC02827; WNK1; CCND2-AS1; RPS6P18; LOC105369625; SLC6A12-AS1; CACNA2D4; LAMP1P1; NINJ2; ADIPOR2; HSPA8P5; RPS26P44; LOC100422463; CRACR2A; CACNA1C-IT3; LOC105369608; LINC00942; CBX3P4; LOC105369594; RPL23AP14; CD9; LOC105369617; LOC103568124; AKAP3; KCNA1; LINC02455; LOC105369611; FOXM1; LOC107984507; PARP11; TEX52; IQSEC3; PRMT8; RPL18P9; LOC107984131; LINC02417; IQSEC3-AS2; LOC101929432; ITFG2; RN7SL69P; ERC1; KCNA5; TEAD4; LOC105369602; CACNA1C-AS2; LOC107984495; LOC105369622; LOC100418939; RNU7-103P; LOC105369616; RPS27P3; TIGAR; LINC02443; RPL13AP24; WNT5B; ITFG2-AS1; RHNO1; LOC105369618; NTF3; LOC105369595; DCP1B; DYRK4; IQSEC3-AS1; KDM5A; NRIP2; LINC00940; CACNA1C-AS1; LOC100128253; C12orf4; NINJ2-AS1; CCDC77; LOC102723544; CACNA1C-AS4; LOC105369601; LOC100533654; OTUD4P1; LOC105369621; LOC107987182; RPS4XP14; CACNA1C-IT1; RNU6-1315P; LOC101901829; FGF23; SLC6A13; CACNA1C; MIR3649; LOC100507560; IQSEC3P1; LOC105369607; FBXL14; VWF; RNU4ATAC16P; GAU1; HTR1DP1; RAD51AP1; FKBP4; KCNA6; LOC105369623; RAD52; LOC100420673; CACNA1C-IT2; LRTM2; B4GALNT3; CCND2; LOC574538; ANO2; LINC02371; NDUFA9; SNORA120; LOC390282; See more...

Location information:

Clinical significance:

ID:: 49622687

variant

11.

nsv3906935

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LRTM2; FOXM1; ANO2; KCNA6; LINC00942; HTR1DP1; LOC103568124; LOC105369594; LOC105369617; LINC02455; AKAP3; LINC02417; ITFG2; LOC101929432; IQSEC3-AS2; RHNO1; RPL18P9; TEAD4; IQSEC3; KCNA5; LOC105369616; PARP11; LOC100418939; RPS27P3; LOC100422463; RNU7-103P; LINC02443; TIGAR; DCP1B; RPL13AP24; LOC105369602; ITFG2-AS1; CACNA1C-AS2; LOC107984495; ADIPOR2; NINJ2-AS1; OTUD4P1; CCDC77; C12orf4; VWF; RPS4XP14; LOC105369618; LOC107987182; RNU6-1315P; LOC105369621; FGF23; LOC105369601; RNU4ATAC16P; KDM5A; DYRK4; CACNA1C-AS4; CACNA1C; NTF3; SLC6A13; MIR3649; LOC100420673; RAD52; IQSEC3P1; PRMT8; LOC105369607; CACNA1C-IT2; TEX52; ERC1; LOC100507560; CACNA1C-IT1; FBXL14; LOC107984131; GAU1; LOC100533654; SLC6A12; CACNA2D4; LOC574538; LOC101901829; LOC390282; NDUFA9; SNORA120; LINC02827; TSPAN9; B4GALNT3; GALNT8; CCND2; FKBP4; THCAT155; RPS15P7; RAD51AP1; LINC02371; CACNA1C-AS1; FGF6; PARP11-AS1; TULP3; LOC105369612; LOC102723544; RNU6-174P; CCND2-AS1; WNT5B; LOC100128253; IQSEC3-AS1; NRIP2; LINC00940; WNK1; RPS6P18; RPS26P44; CRACR2A; CACNA1C-IT3; LOC107984507; HSPA8P5; LOC105369595; LAMP1P1; RPL23AP14; LOC105369611; NINJ2; KCNA1; LOC105369608; CBX3P4; SLC6A12-AS1; See more...

Location information:

Clinical significance:

ID:: 48470290

variant

12.

nsv3907924

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: SLC6A13; RPL18P9; CACNA1C; IQSEC3; LOC105369607; LOC107984131; ERC1; IQSEC3-AS2; IQSEC3P1; LOC101929432; TEAD4; PRMT8; TEX52; ITFG2; CACNA1C-IT2; GALNT8; TSPAN9; RPS15P7; FGF6; SLC6A12; THCAT155; TULP3; PARP11-AS1; RPS6P18; WNK1; CACNA2D4; CCND2-AS1; LINC02827; RNU6-174P; WNT5B; LINC00940; KDM5A; NTF3; CACNA1C-AS4; LOC105369618; LOC105369612; CCDC77; IQSEC3-AS1; CACNA1C-AS1; DYRK4; OTUD4P1; LOC105369595; NINJ2-AS1; LOC102723544; NRIP2; LOC100128253; LINC00942; KCNA1; RPL23AP14; LOC103568124; NINJ2; AKAP3; HSPA8P5; LOC105369594; LOC107984507; LOC105369611; LINC02371; CBX3P4; LINC02455; LOC105369617; FKBP4; LOC390282; LOC574538; LRTM2; FOXM1; NDUFA9; KCNA6; ANO2; RAD51AP1; HTR1DP1; LOC100418939; B4GALNT3; CCND2; LINC02417; LOC105369616; RHNO1; LINC02443; LOC107984495; RPS27P3; TIGAR; DCP1B; CACNA1C-AS2; PARP11; RPL13AP24; KCNA5; ADIPOR2; LOC100422463; RPS26P44; RNU7-103P; ITFG2-AS1; LOC105369602; SLC6A12-AS1; LAMP1P1; LOC105369608; CRACR2A; RNU6-1315P; GAU1; FGF23; LOC101901829; LOC105369621; CACNA1C-IT3; RNU4ATAC16P; FBXL14; LOC100420673; RPS4XP14; LOC107987182; LOC100533654; CACNA1C-IT1; RAD52; MIR3649; C12orf4; LOC100507560; LOC105369601; See more...

Location information:

Clinical significance:

ID:: 48471279

variant

13.

nsv3901202

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105369595; KDM5A; IQSEC3-AS1; NTF3; DYRK4; OTUD4P1; LOC105369618; LINC00940; CACNA1C-AS4; C12orf4; RPS4XP14; LOC100128253; WNT5B; NINJ2-AS1; NRIP2; CACNA1C-AS1; CCDC77; LOC103568124; LOC102723544; LINC02455; CBX3P4; LOC105369594; KCNA1; LOC105369617; RPL23AP14; LINC00942; AKAP3; LOC105369611; LOC107984507; FOXM1; FKBP4; LINC02371; RAD51AP1; KCNA6; ANO2; LOC574538; CCND2; HTR1DP1; LRTM2; NDUFA9; B4GALNT3; LOC390282; LOC100418939; RNU7-103P; LOC107984495; LOC105369616; CACNA1C-AS2; LOC105369602; KCNA5; ITFG2-AS1; DCP1B; RHNO1; RPL13AP24; TIGAR; LINC02443; RPS27P3; LAMP1P1; RPS26P44; ADIPOR2; CRACR2A; SLC6A12-AS1; HSPA8P5; CACNA1C-IT3; LOC100422463; FBXL14; GAU1; FGF23; LOC105369608; LOC100533654; RNU4ATAC16P; LOC105369601; NINJ2; CACNA1C; SLC6A13; CACNA1C-IT2; RAD52; LOC101901829; LOC107987182; RNU6-1315P; CACNA1C-IT1; LOC105369607; LOC100420673; IQSEC3P1; LOC107984131; MIR3649; IQSEC3; TEX52; IQSEC3-AS2; LOC100507560; PARP11; LINC02417; LOC101929432; TEAD4; RPL18P9; THCAT155; RNU6-174P; ERC1; RPS15P7; ITFG2; TSPAN9; GALNT8; PRMT8; LINC02827; CACNA2D4; CCND2-AS1; SLC6A12; TULP3; LOC105369612; PARP11-AS1; FGF6; RPS6P18; WNK1; See more...

Location information:

Clinical significance:

ID:: 48464557

variant

14.

nsv4729176

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RPL18P9; CACNA1C; SLC6A13; MIR3649; LOC105369607; FBXL14; IQSEC3P1; LOC107984131; PRMT8; ERC1; CACNA1C-IT2; RAD52; TEX52; CACNA1C-IT1; RNU6-1315P; LOC100533654; CACNA1C-AS4; FGF23; KDM5A; OTUD4P1; DYRK4; RNU4ATAC16P; C12orf4; RPS4XP14; LOC107987182; LOC105369601; LINC00940; WNT5B; CCDC77; IQSEC3-AS1; CACNA1C-AS1; LOC105369595; LOC105369612; LOC102723544; RPS6P18; WNK1; CCND2-AS1; NINJ2-AS1; NRIP2; RNU6-174P; TULP3; LOC100128253; FGF6; RPS15P7; TSPAN9; LINC02371; SLC6A12; THCAT155; PARP11-AS1; CACNA2D4; B4GALNT3; LINC02827; RAD51AP1; LINC00942; FKBP4; LINC02455; LOC574538; LRTM2; LOC105369594; FOXM1; HTR1DP1; RPS26P44; HSPA8P5; NINJ2; RPL23AP14; CCND2; LAMP1P1; LOC107984507; LOC105369611; LOC105369608; CBX3P4; SLC6A12-AS1; CACNA1C-IT3; ADIPOR2; TIGAR; LOC100422463; LOC105369602; DCP1B; LOC107984495; ITFG2-AS1; CRACR2A; RNU7-103P; IQSEC3; RPL13AP24; IQSEC3-AS2; LINC02417; RPS27P3; LOC101929432; TEAD4; RHNO1; PARP11; CACNA1C-AS2; LOC100418939; ITFG2; See more...

Location information:

Clinical significance:

ID:: 50372813

variant

15.

nsv3912688

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: RPL23AP14; CRACR2A; HSPA8P5; RPS26P44; CACNA1C-IT3; LOC105369611; NINJ2; LAMP1P1; LOC105369608; LOC107984507; CBX3P4; SLC6A12-AS1; LOC105369595; LOC105369612; LINC00940; LOC102723544; CCND2-AS1; IQSEC3-AS1; CACNA1C-AS1; WNK1; PARP11-AS1; RPS6P18; LOC100128253; NRIP2; WNT5B; RNU6-174P; RPS15P7; TULP3; LINC02371; THCAT155; FKBP4; SLC6A12; LINC02827; LOC574538; B4GALNT3; CACNA2D4; CCND2; TSPAN9; FBXL14; CACNA1C-IT1; CACNA1C; LOC107984131; SLC6A13; PRMT8; CACNA1C-IT2; ERC1; RAD52; LOC105369607; MIR3649; IQSEC3P1; RNU4ATAC16P; LOC100533654; TEX52; KDM5A; FGF23; CACNA1C-AS4; RNU6-1315P; CCDC77; OTUD4P1; NINJ2-AS1; RPS4XP14; LOC107987182; LOC105369601; TIGAR; ITFG2-AS1; ADIPOR2; LOC107984495; RPS27P3; LOC100422463; DCP1B; CACNA1C-AS2; LOC105369602; RNU7-103P; RPL13AP24; IQSEC3; LINC02417; IQSEC3-AS2; TEAD4; LOC100418939; LOC101929432; PARP11; ITFG2; RHNO1; RPL18P9; HTR1DP1; LINC00942; LINC02455; LOC105369594; LRTM2; FOXM1; See more...

Location information:

Clinical significance:

ID:: 48476043

variant

16.

nsv3916748

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LAMP1P1; RPL23AP14; CBX3P4; CACNA1C-IT3; LOC105369594; LOC107984507; LOC105369608; NINJ2; WNT5B; CACNA1C-AS4; LOC105369595; LINC00940; NRIP2; LOC100128253; RNU6-174P; LOC102723544; RPS6P18; WNK1; CCDC77; IQSEC3-AS1; CACNA1C-AS1; NINJ2-AS1; LINC02371; TULP3; TSPAN9; PARP11-AS1; LINC02827; B4GALNT3; CACNA2D4; THCAT155; SLC6A12; RAD52; TEX52; CACNA1C-IT2; LOC105369607; IQSEC3P1; ERC1; LOC107984131; SLC6A13; PRMT8; CACNA1C; KDM5A; RNU6-1315P; CACNA1C-IT1; FBXL14; LOC107987182; LOC100533654; RPS4XP14; LOC105369601; RNU4ATAC16P; MIR3649; OTUD4P1; SLC6A12-AS1; ADIPOR2; LOC107984495; ITFG2-AS1; LOC100422463; DCP1B; LOC105369602; RPL13AP24; RPS26P44; RNU7-103P; LOC100418939; IQSEC3; CRACR2A; PARP11; TEAD4; ITFG2; RHNO1; CACNA1C-AS2; IQSEC3-AS2; RPS27P3; LINC02417; LINC02455; FKBP4; LOC101929432; LINC00942; HTR1DP1; LOC574538; FOXM1; LRTM2; See more...

Location information:

Clinical significance:

ID:: 48480103

variant

17.

nsv3909356

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: ITFG2-AS1; LOC105369602; RPL13AP24; DCP1B; RHNO1; CACNA1C-AS2; LOC107984495; LOC100418939; RNU7-103P; RPS27P3; NRIP2; RPS4XP14; LOC100128253; LINC00940; WNT5B; LOC105369595; KDM5A; OTUD4P1; IQSEC3-AS1; CACNA1C-AS4; LOC102723544; CACNA1C-AS1; NINJ2-AS1; CCDC77; RAD52; LOC105369607; CACNA1C-IT2; LOC100533654; LOC105369601; CACNA1C-IT1; LOC107987182; RNU6-1315P; FBXL14; CACNA1C; RNU4ATAC16P; IQSEC3P1; SLC6A13; MIR3649; HTR1DP1; LOC574538; LINC02371; FKBP4; LRTM2; B4GALNT3; LINC02827; CACNA2D4; TSPAN9; RPS6P18; RNU6-174P; WNK1; THCAT155; SLC6A12; TULP3; PARP11-AS1; LAMP1P1; ADIPOR2; CACNA1C-IT3; LOC105369608; SLC6A12-AS1; CRACR2A; LOC100422463; RPS26P44; LOC107984507; LINC00942; NINJ2; LOC105369594; LINC02455; RPL23AP14; CBX3P4; FOXM1; ERC1; LOC101929432; TEX52; LOC107984131; IQSEC3; PARP11; TEAD4; IQSEC3-AS2; ITFG2; PRMT8; LINC02417; See more...

Location information:

Clinical significance:

ID:: 48472711

variant

18.

nsv3910104

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DCP1B; RPL13AP24; ITFG2-AS1; CACNA1C-AS2; ADIPOR2; LOC105369602; LOC100422463; RNU7-103P; RPS27P3; LOC107984495; RPS4XP14; RNU6-1315P; LOC105369601; CACNA1C-AS4; LOC107987182; KDM5A; LOC105369595; CCDC77; OTUD4P1; NINJ2-AS1; ERC1; RAD52; CACNA1C-IT2; LOC105369607; CACNA1C-IT1; LOC100533654; TEX52; LOC107984131; CACNA1C; RNU4ATAC16P; IQSEC3P1; SLC6A13; FBXL14; MIR3649; PRMT8; CACNA2D4; LINC02827; LOC574538; LINC02371; TSPAN9; TULP3; FKBP4; THCAT155; B4GALNT3; SLC6A12; LOC100128253; RPS6P18; WNT5B; NRIP2; LINC00940; IQSEC3-AS1; CACNA1C-AS1; WNK1; RNU6-174P; CACNA1C-IT3; LOC102723544; PARP11-AS1; CBX3P4; RPL23AP14; SLC6A12-AS1; LAMP1P1; CRACR2A; RPS26P44; NINJ2; LOC105369608; HTR1DP1; LOC107984507; LINC00942; LINC02455; FOXM1; LOC105369594; LRTM2; ITFG2; LOC101929432; IQSEC3; LOC100418939; LINC02417; RHNO1; PARP11; TEAD4; See more...

Location information:

Clinical significance:

ID:: 48473459

variant

19.

nsv3894971

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CRACR2A; LOC107984495; RPL13AP24; LOC100422463; ITFG2-AS1; DCP1B; RNU7-103P; LOC105369602; ADIPOR2; LOC100418939; LINC02417; IQSEC3; TEAD4; RPS27P3; RHNO1; LOC101929432; ITFG2; CACNA1C-AS2; PARP11; SLC6A13; LOC107984131; CACNA1C; FBXL14; PRMT8; IQSEC3P1; MIR3649; RAD52; CACNA1C-IT2; LOC105369607; ERC1; TEX52; RNU6-1315P; KDM5A; RNU4ATAC16P; RPS4XP14; CACNA1C-AS4; CACNA1C-IT1; LOC100533654; LOC107987182; LOC105369595; LOC105369601; IQSEC3-AS1; CACNA1C-AS1; WNK1; NINJ2-AS1; LOC102723544; CCDC77; LOC100128253; NRIP2; RPS6P18; WNT5B; LINC00940; RNU6-174P; THCAT155; SLC6A12; B4GALNT3; LINC02827; LINC02371; TULP3; CACNA2D4; TSPAN9; FKBP4; LOC105369594; LINC02455; HTR1DP1; LOC574538; FOXM1; LRTM2; LINC00942; RPS26P44; NINJ2; LOC107984507; RPL23AP14; LAMP1P1; CACNA1C-IT3; SLC6A12-AS1; CBX3P4; See more...

Location information:

Clinical significance:

ID:: 48458326

variant

20.

nsv3914833

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: NRIP2; RPS4XP14; LINC00940; WNT5B; LOC100128253; CACNA1C-AS1; KDM5A; LOC102723544; NINJ2-AS1; CACNA1C-AS4; CCDC77; LOC105369595; DCP1B; RHNO1; CACNA1C-AS2; LOC105369602; ITFG2-AS1; RPL13AP24; RNU7-103P; RPS27P3; LOC100418939; TEX52; ERC1; ITFG2; LOC101929432; IQSEC3; TEAD4; LINC02417; PRMT8; IQSEC3-AS2; LOC107984131; LINC00942; CBX3P4; LOC107984507; RPL23AP14; LOC105369594; LINC02455; FOXM1; LAMP1P1; SLC6A12-AS1; CACNA1C-IT3; ADIPOR2; NINJ2; RPS26P44; LOC100422463; CRACR2A; CACNA2D4; TULP3; RPS6P18; IQSEC3-AS1; LINC02827; TSPAN9; SLC6A12; WNK1; LOC574538; THCAT155; HTR1DP1; LRTM2; FKBP4; B4GALNT3; LOC107987182; LOC100533654; LOC105369601; LOC105369607; CACNA1C-IT1; MIR3649; LINC02371; IQSEC3P1; CACNA1C; RAD52; SLC6A13; RNU6-1315P; CACNA1C-IT2; FBXL14; RNU4ATAC16P; See more...

Location information:

Clinical significance:

ID:: 48478188

variant

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iqsec3[All Fields] AND 1[has_clinical] (77)
dbVar
Rattus norvegicus MOB kinase activator 2 (Mob2), mRNA
Rattus norvegicus MOB kinase activator 2 (Mob2), mRNA
gi|1939401959|ref|NM_001109159.2|

Nucleotide
Eif4a-ps5 eukaryotic translation initiation factor 4A, pseudogene 5 [Mus musculu...
Eif4a-ps5 eukaryotic translation initiation factor 4A, pseudogene 5 [Mus musculus]
Gene ID:108275

Gene

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