NRGN - dbVar - NCBI

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1.

Variant type:: copy number variation

Associated study:: estd209

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 14214041

variant

2.

Variant type:: insertion

Associated study:: estd194

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 6469045

variant

3.

Variant type:: insertion

Associated study:: estd22

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 8177309

variant

4.

Variant type:: short tandem repeat

Associated study:: nstd128

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 35378952

variant

5.

Variant type:: short tandem repeat

Associated study:: nstd128

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 35380436

variant

6.

Variant type:: short tandem repeat

Associated study:: nstd128

Organism:
human

Genes(s) in region:: NRGN

Location information:

ID:: 35385428

variant

7.

Variant type:: copy number variation

Associated study:: nstd73

Organism:
human

Genes(s) in region:: NRGN; VSIG2

Location information:

ID:: 13390501

variant

8.

Variant type:: translocation

Associated study:: nstd200

Organism:
human

Genes(s) in region:: VSIG2; NRGN

Location information:

ID:: 51602071

variant

9.

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: MSANTD2; VSIG2; ESAM-AS1; NRGN; ESAM

Location information:

ID:: 9594331

variant

10.

Variant type:: copy number variation

Associated study:: nstd54

Organism:
human

Genes(s) in region:: ESAM-AS1; MSANTD2; NRGN; VSIG2; ESAM

Location information:

ID:: 3835203

variant

11.

Variant type:: copy number variation

Associated study:: estd219

Organism:
human

Genes(s) in region:: VSIG2; ESAM; NRGN

Location information:

ID:: 45761856

variant

12.

Variant type:: copy number variation

Associated study:: estd214

Organism:
human

Genes(s) in region:: VSIG2; NRGN; ESAM

Location information:

ID:: 24477959

variant

13.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PHB1P17; KIRREL3; LOC107984407; NFRKB; DNAJB6P1; B3GAT1-DT; OR8A2P; LINC02744; DCPS; OR10D5P; SORL1; TRIM29; ETS1; OR10D1P; RN7SL778P; LOC105369551; LOC105369531; LOC649133; LOC100533644; LOC105369568; LOC105369574; CHEK1; LOC105369591; PKNOX2; PATE4; OR8B1P; LOC107984404; OR6T1; RPL34P21; GRIK4; LOC105369571; LOC101929473; FOXRED1; LINC02717; TMEM218; SAE1P1; OR8D2; ELOCP22; RN7SKP121; ESAM; ST3GAL4; POU2F3; TBRG1; RPS26P43; RNU6-876P; BARX2; LOC105369530; OR6M3P; RNU6-321P; PATE2; LOC105378956; SF3A3P2; RN7SKP279; NRGN; OR10D3; OR8F1P; CCDC15-DT; LOC105369527; OR10D4P; PATE3; LOC107984400; STT3A-AS1; TIRAP; LOC107984357; LOC105369544; MIR4493; OR10S1; SCN3B; SNORD153; KCNJ5-AS1; FAM118B; OR10G9; RPS4XP12; OR8D1; PATE1; PUS3; LOC105369587; OR8D4; LOC107984409; KCNJ1; VWA5A; LOC107984432; LOC107984412; CCDC15; LOC105369533; LOC105369576; MIR3167; DUXAP5; LINC02743; ROBO4; ZBTB44; CDON; THY1; LOC107984406; OR10G6; TBCEL; RN7SL167P; OR8X1P; BAK1P2; TLCD5; TECTA; LOC101929538; MSANTD2-AS1; KIRREL3-AS3; OR8A3P; MIR4697; B3GAT1; OR8B4; SORL1-AS1; TP53AIP1; NECTIN1-DT; LOC390255; OR8A1; LOC105369559; KRT8P7; ACRV1; SIAE; LOC105369579; LOC105369532; OR8B5P; RNU4-23P; OR8B3; SLC37A2; USP2-AS1; PRDM10-DT; ARHGEF12; LOC100507548; LOC105369575; LOC101929208; SRPRA; GSEC; LOC105369535; TMEM225; LOC105369529; NECTIN1; LOC107984405; KIRREL3-AS2; PKNOX2-AS1; ZNF202; OR8B12; MIRLET7A2; UBASH3B; OR8G7P; THYN1; LOC105369572; ETS1-AS1; SPATA19; VSIG10L2; LOC100421417; LINC02712; LOC100419058; OR8B6P; RNU2-35P; LINC01395; OR4D5; JHY; RNU6ATAC12P; HEPACAM; LOC399975; RNU6-874P; ROBO3; OR8B10P; RNU6-1156P; HYLS1; OR8G1; JAM3; APLP2; SNORD14C; LOC107984411; OR10G5P; RN7SL351P; PKNOX2-DT; BMPR1AP2; STT3A; LINC02706; GLB1L3; CLMP; OR6X1; LINC02098; MSANTD2; MIR6090; LINC02551; RPL34P23; NAP1L1P1; RNU1-21P; ARHGAP32; LOC107984374; LOC105369578; LOC105369558; RNU6-256P; LINC02731; LINC02727; LOC105369561; MIR125B1; ACAD8; LOC105369577; LINC02730; ESAM-AS1; DDX18P5; RNA5SP352; RPL31P47; RNU4-86P; BLID; LOC101929227; MIR8052; LOC105369534; VPS26B; LOC105369520; OR8B8; LOC107984413; GRAMD1B; HEPN1; OR8B7P; LOC107984373; RPS27P20; RNU6-592P; RNU4ATAC5P; LOC107984350; LOC105369540; RPUSD4; BSX; LOC403312; TMEM45B; TRK-TTT2-1; ADAMTS15; LOC105369580; LINC02714; NCAPD3; LOC283172; LOC105369526; DDX25; OR8C1P; TIRAP-AS1; KCNJ5; LOC105369543; RNU4ATAC10P; ZNF123P; OR8G3P; SLC5A4P1; PANX3; ST14; LOC107984402; ATP5PBP5; ZBTB44-DT; PPP1R10P1; LOC107984399; LOC107984379; NTM-AS1; PTP4A2P2; OR8Q1P; LINC02725; NDUFAF2P2; RPL35AP26; OR10G7; RNU6-1123P; LINC02684; OR8G5; LOC101929653; SPA17; OR6M2P; LINC02697; SC5D; ADAMTS8; ELOBP2; EI24; LOC112268069; SENCR; KRT18P59; OR10G4; OR10N1P; HMGB1P42; LOC105369583; LINC02873; OR10G8; OAF; LOC105369565; LOC105369545; PRDM10; LOC105369562; CRTAM; SNORD14E; FEZ1; LOC105369539; OR8B9P; SNORD14D; LOC100421985; LOC107984398; GLULP3; OR6M1; MIR100; FLI1; OPCML; LOC102724410; SNX19; IGSF9B; VSIG2; HSPA8; MIR10526; NECTIN1-AS1; OR8G2P; OR8B2; MIR100HG; LOC101929427; NTM; GLB1L2; NTM-IT; See more...

Location information:

Clinical significance:

ID:: 48474364

variant

14.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: ETS1-AS1; SLC37A2; THYN1; VSIG10L2; LOC100421417; SPATA19; ARHGEF12; LINC02712; SIAE; LOC100507548; LOC105369532; OR4D5; LINC01395; HEPACAM; ACRV1; LOC105369578; LOC105369535; LOC105369575; OR8B6P; RNU6ATAC12P; RNU4-23P; USP2-AS1; PRDM10-DT; ZNF202; JHY; SRPRA; KRT8P7; OR8B10P; MIRLET7A2; KIRREL3-AS2; LOC399975; PKNOX2-DT; LOC101929208; OR8B12; LOC107984405; OR8G7P; GSEC; NECTIN1; LINC02697; LOC105369572; LOC105369529; ZNF123P; LOC105369543; ST14; LOC107984379; LOC107984402; ZBTB44-DT; LOC107984399; LINC02725; LOC100419058; PTP4A2P2; OR10G8; RNU2-35P; OR6M2P; NDUFAF2P2; OR8G3P; SNORD14E; RNU6-1123P; NTM-AS1; OR8B3; DDX25; RNU4ATAC10P; ATP5PBP5; TMEM225; PKNOX2-AS1; OR8C1P; RPL35AP26; UBASH3B; PPP1R10P1; LOC105369526; OR10G7; SLC5A4P1; PANX3; ADAMTS15; BLID; RPS27P20; BSX; OR8Q1P; SPA17; LOC105369580; TMEM45B; HEPN1; LINC02714; LOC105369520; LOC105369540; LOC105369583; LOC107984373; KCNJ5; LOC107984413; LOC403312; GRAMD1B; ACAD8; NCAPD3; LOC107984350; LOC105369577; RNU4-86P; VPS26B; TIRAP-AS1; MIR8052; RNA5SP352; RNU4ATAC5P; RPL31P47; RNU6-592P; LOC283172; OR8B8; LOC105369568; TRK-TTT2-1; ESAM; LOC101929473; DCPS; OR8D2; TMEM218; CHEK1; OR6T1; LOC100533644; OR8A2P; ELOCP22; OR8B7P; RPUSD4; RPL34P21; SORL1; TRIM29; LOC105369574; ETS1; PATE4; LOC105369534; PHB1P17; LOC649133; OR10D5P; LOC105369571; RN7SL778P; ST3GAL4; LOC105369531; NFRKB; LOC105369591; LOC101929227; LINC02744; DNAJB6P1; LOC107984407; SAE1P1; LOC105369565; LOC105369545; CRTAM; OR8B1P; PKNOX2; FOXRED1; LINC02717; LOC105369551; LOC107984404; NTM-IT; OR8B9P; FEZ1; OAF; GLULP3; LOC102724410; RN7SKP121; MIR100; LOC105369562; OPCML; NECTIN1-AS1; LOC107984398; IGSF9B; OR8G2P; LOC100421985; OR8G5; SNORD14D; MIR10526; SC5D; LOC101929427; GLB1L2; NTM; ELOBP2; GRIK4; OR10D1P; EI24; KRT18P59; OR10G4; B3GAT1-DT; FLI1; HSPA8; PRDM10; OR10N1P; SENCR; LINC02873; MSANTD2-AS1; ADAMTS8; LOC101929653; LOC101929538; DUXAP5; OR6M1; VSIG2; KIRREL3; LOC105369539; NECTIN1-DT; LOC105369559; OR8A3P; BAK1P2; KIRREL3-AS3; LOC107984409; MIR100HG; LOC107984412; OR8B2; LOC105369533; HMGB1P42; LOC390255; LOC105369579; SORL1-AS1; LOC112268069; OR10G6; OR8A1; LOC107984432; SNX19; MIR3167; TP53AIP1; LINC02743; LOC105369576; ROBO4; ZBTB44; RN7SL167P; MIR4697; LOC107984406; PATE3; OR8B5P; VWA5A; LOC107984357; TLCD5; TBCEL; OR8X1P; SNORD153; KCNJ5-AS1; LOC107984400; RPS4XP12; OR8B4; SCN3B; CDON; POU2F3; OR8D1; OR10S1; TECTA; FAM118B; OR10G9; OR8D4; RPS26P43; PATE1; KCNJ1; LOC105378956; PUS3; TBRG1; CCDC15; LOC105369530; RNU6-321P; B3GAT1; LOC105369527; BARX2; STT3A-AS1; RN7SKP279; OR6M3P; SF3A3P2; NRGN; MIR4493; CCDC15-DT; PATE2; OR6X1; TIRAP; LINC02551; STT3A; OR8F1P; LINC02731; RNU1-21P; NAP1L1P1; LOC107984374; LOC105369558; RNU6-256P; LINC02706; MIR125B1; CLMP; LOC105369544; ARHGAP32; RNU6-874P; MSANTD2; ROBO3; HYLS1; APLP2; OR8G1; RNU6-1156P; OR10D4P; LOC107984411; JAM3; RPL34P23; OR10D3; LINC02730; OR10G5P; SNORD14C; LINC02098; ESAM-AS1; LINC02727; DDX18P5; LOC105369561; BMPR1AP2; GLB1L3; MIR6090; RNU6-876P; RN7SL351P; See more...

Location information:

Clinical significance:

ID:: 48486128

variant

15.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: TMEM225; OR6M2P; LINC01395; LOC105369532; OR8B3; RNU4-23P; RNU2-35P; JHY; LOC105369529; NTM-AS1; OR8B10P; LOC100507548; RNU6ATAC12P; LOC105369526; GSEC; MIRLET7A2; LOC107984405; OR8G7P; PRDM10-DT; KIRREL3-AS2; ZNF202; LOC105369572; UBASH3B; LOC107984379; PKNOX2-AS1; SRPRA; NECTIN1; SLC37A2; ZNF123P; LOC107984402; SPATA19; OR4D5; OR8G3P; OR8D2; LOC100419058; ETS1-AS1; OR10D1P; OPCML; LOC101929473; B3GAT1-DT; PHB1P17; SNORD14D; RN7SL778P; LOC101929427; ETS1; OR8A2P; TRIM29; ELOBP2; GRIK4; PATE4; LOC105369571; EI24; PKNOX2; KIRREL3; VSIG2; KRT18P59; NFRKB; LINC02744; LOC105369568; OR8B9P; TMEM218; LOC105369545; ESAM; RN7SKP121; LOC107984404; NECTIN1-AS1; LOC649133; OR8B1P; OR10N1P; LOC105369591; FOXRED1; OR6T1; CHEK1; LINC02717; LOC105369565; RPS27P20; LINC02714; ELOCP22; RPL34P21; RPUSD4; KCNJ5; OR8B7P; LOC105369574; SORL1; GRAMD1B; LOC105369534; TIRAP-AS1; LOC105369577; LOC107984407; ST3GAL4; VPS26B; OR10D5P; RNA5SP352; RNU4-86P; LOC105369531; DNAJB6P1; LOC101929227; DCPS; LOC105369551; MIR8052; TRK-TTT2-1; LOC100533644; SAE1P1; RNU4ATAC5P; BLID; BSX; OR8A1; OR8B4; LOC105369533; OR8D1; PATE1; LOC390255; MIR4697; LOC105369576; CCDC15; TBRG1; LOC105378956; ROBO4; OR8D4; KCNJ1; STT3A-AS1; ZBTB44; LOC107984409; RN7SL167P; OR6M3P; OR10G6; LOC107984406; LOC105369530; TECTA; TBCEL; NRGN; PATE3; SF3A3P2; LOC101929538; LOC105369559; OR8A3P; SNX19; KCNJ5-AS1; LOC105369562; GLB1L2; MIR100HG; NTM-IT; B3GAT1; KIRREL3-AS3; CDON; LOC102724410; OR8X1P; TP53AIP1; FEZ1; NTM; SC5D; MIR100; HSPA8; NECTIN1-DT; LOC100421985; SORL1-AS1; MIR3167; FLI1; MIR10526; OR8G5; LOC105369579; LOC107984432; OR8B5P; LINC02743; OR10G4; IGSF9B; LOC112268069; LOC105369539; LOC107984412; PRDM10; VWA5A; OR8G2P; LOC101929653; OR8B2; CRTAM; LINC02873; SENCR; OR6M1; ADAMTS8; OR8B6P; MSANTD2-AS1; HEPACAM; RNU6-256P; TLCD5; BAK1P2; HMGB1P42; LOC399975; ACRV1; LOC101929208; GLULP3; DDX18P5; OAF; LOC105369575; MSANTD2; JAM3; LOC105369535; VSIG10L2; LOC105369561; LOC105369578; GLB1L3; MIR125B1; STT3A; LOC105369558; ARHGEF12; RNU6-1156P; SIAE; LINC02712; PKNOX2-DT; MIR6090; OR8B12; LOC107984411; APLP2; RNU6-874P; ROBO3; OR10G5P; LINC02731; HYLS1; LINC02730; RPS4XP12; LOC100421417; THYN1; NAP1L1P1; LOC107984374; LINC02551; RNU1-21P; SCN3B; FAM118B; RPL34P23; OR6X1; ARHGAP32; CLMP; RPS26P43; LINC02727; ESAM-AS1; BMPR1AP2; LOC105369527; RNU6-321P; OR8G1; SNORD153; LINC02706; RNU6-876P; BARX2; OR10D3; CCDC15-DT; PUS3; OR10G9; PATE2; POU2F3; LOC107984400; LOC105369544; TIRAP; SNORD14C; LINC02725; LINC02098; LOC107984357; OR10G8; LOC105369540; HEPN1; OR10D4P; MIR4493; NDUFAF2P2; LOC105369580; LOC107984373; RN7SL351P; RN7SKP279; OR8F1P; LOC107984413; LOC105369583; SNORD14E; OR10S1; NCAPD3; LOC403312; ACAD8; RPL31P47; LOC105369587; PPP1R10P1; RNU4ATAC10P; PTP4A2P2; RPL35AP26; LOC283172; OR8C1P; LOC105369543; OR10G7; ZBTB44-DT; SPA17; ADAMTS15; TMEM45B; LINC02697; RNU6-592P; ST14; LOC107984399; LOC107984350; DDX25; PANX3; SLC5A4P1; OR8Q1P; OR8B8; ATP5PBP5; See more...

Location information:

Clinical significance:

ID:: 48470198

variant

16.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: FEZ1; OR6M1; OR10G4; SNX19; OR8B2; CRTAM; LOC105369562; IGSF9B; ZBTB44; OR8B5P; MIR10526; PRDM10; MSANTD2-AS1; MIR100HG; OR8X1P; HMGB1P42; LOC107984409; GLULP3; MIR3167; VWA5A; LINC02873; SENCR; OR8G2P; OAF; BAK1P2; LOC107984412; LOC112268069; LOC107984432; TLCD5; TP53AIP1; LINC02743; LOC105369539; SORL1-AS1; LOC100421985; LOC105369559; OR8G5; NTM-IT; GLB1L2; RNU6-256P; NTM; STT3A; LOC100421417; LINC02551; LOC105369579; ETS1-AS1; VSIG10L2; JHY; HEPACAM; LINC02712; JAM3; OR6X1; ARHGEF12; OR8B12; THYN1; RNU1-21P; ACRV1; RPL34P23; LINC02731; MIR6090; GLB1L3; LOC105369575; LOC105369532; RNU6-1156P; OR10G5P; CLMP; LOC101929208; PKNOX2-DT; SIAE; LOC107984411; MSANTD2; RNU6-874P; LOC105369558; LOC105369578; LOC105369535; ROBO3; LOC399975; OR8B6P; MIRLET7A2; LINC02727; OR10G9; LINC02098; LOC107984357; LOC107984400; ARHGAP32; LOC105369544; TIRAP; LOC105369561; LINC02706; SNORD153; OR10D4P; RNU6-876P; POU2F3; BARX2; CCDC15-DT; PATE2; OR8G1; RNU6-321P; MIR4493; BMPR1AP2; RN7SL351P; RN7SKP279; OR8F1P; RPS26P43; OR10D3; HYLS1; SNORD14C; MIR125B1; NAP1L1P1; DDX18P5; ESAM-AS1; SCN3B; LOC107984374; LINC02730; APLP2; FAM118B; LINC02697; LINC02725; TMEM45B; LOC105369543; RPL35AP26; SPA17; ZBTB44-DT; ST14; OR8B8; LOC105369540; OR8Q1P; RNU6-592P; LOC105369583; OR10G7; PTP4A2P2; BLID; RPL31P47; RNU4-86P; ATP5PBP5; SLC5A4P1; ADAMTS15; PPP1R10P1; LOC403312; MIR8052; NCAPD3; LOC105369580; LOC107984350; LOC283172; LOC107984373; LOC107984413; DDX25; HEPN1; LOC107984379; NDUFAF2P2; ACAD8; OR10G8; SPATA19; SNORD14E; RNU2-35P; ZNF123P; OR6M2P; LOC107984405; LOC107984402; LOC100419058; ZNF202; OR8C1P; OR8G7P; LINC01395; LOC105369526; PKNOX2-AS1; LOC107984399; PANX3; OR8G3P; SLC37A2; PRDM10-DT; LOC105369529; OR4D5; NTM-AS1; LOC100507548; TMEM225; SRPRA; GSEC; UBASH3B; RNU4ATAC10P; OR8B3; RNU6ATAC12P; KIRREL3-AS2; LOC105369572; OPCML; RNU4-23P; LINC02744; LOC105369545; OR8B1P; LOC105369565; FOXRED1; OR8B10P; OR10D1P; OR8B9P; ADAMTS8; ELOBP2; OR6T1; GRIK4; LOC649133; CHEK1; FLI1; LOC105369568; B3GAT1-DT; LOC101929653; RN7SL778P; RN7SKP121; LOC102724410; LOC101929427; LINC02717; PKNOX2; ESAM; HSPA8; VSIG2; EI24; KRT18P59; LOC105369591; PHB1P17; KIRREL3; PATE4; BSX; TRIM29; OR10N1P; SC5D; LOC101929473; DCPS; RPL34P21; SNORD14D; LOC107984404; MIR100; DNAJB6P1; TMEM218; TRK-TTT2-1; RNU4ATAC5P; GRAMD1B; LOC107984407; OR10D5P; NFRKB; ETS1; LOC105369571; LOC105369551; LOC105369534; LOC105369574; RPS27P20; LOC105369531; LOC105369577; ST3GAL4; KCNJ5; ELOCP22; LOC101929227; RPUSD4; TIRAP-AS1; LINC02714; RNA5SP352; LOC100533644; SAE1P1; OR8A2P; OR8D2; OR8B7P; SORL1; MIR4697; OR8B4; OR8A3P; OR10S1; KIRREL3-AS3; PUS3; RN7SL167P; VPS26B; CDON; OR10G6; TBCEL; NRGN; B3GAT1; KCNJ5-AS1; TBRG1; TECTA; LOC105369576; OR6M3P; CCDC15; OR8A1; KCNJ1; SF3A3P2; LOC105378956; PATE1; LOC105369533; LOC101929538; PATE3; LOC105369527; STT3A-AS1; LOC107984406; LOC105369530; ROBO4; RPS4XP12; OR8D4; OR8D1; See more...

Location information:

Clinical significance:

ID:: 48466030

variant

17.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: KIRREL3-AS3; OR8B4; MIR4697; SORL1-AS1; LOC101929538; PATE1; OR8A3P; OR8D4; OR8A1; LOC105369533; OR8B5P; OR6M3P; LOC105369576; CCDC15; LOC107984409; KCNJ1; SF3A3P2; OR10G6; ROBO4; CDON; TECTA; KCNJ5-AS1; TBRG1; VWA5A; TBCEL; LOC107984357; TIRAP; ZBTB44; LOC107984406; STT3A-AS1; OR8X1P; LOC107984400; B3GAT1; RN7SL167P; OR8D1; LINC02706; LOC105369544; LOC105369587; SCN3B; LINC02098; ARHGAP32; SNORD153; FAM118B; ESAM-AS1; OR10S1; NAP1L1P1; OR10G9; RN7SKP279; RPS26P43; SNORD14C; OR10D3; PUS3; OR8F1P; RPS4XP12; RN7SL351P; BARX2; PATE2; RNU6-321P; MIR4493; RNU6-876P; OR10D4P; PATE3; CCDC15-DT; NRGN; LOC100421417; LINC02551; OR6X1; VSIG10L2; LINC02727; RNU1-21P; STT3A; RPL34P23; HEPACAM; HYLS1; LOC105369558; LINC02730; LOC107984374; LOC105369535; DDX18P5; LOC105369578; LOC399975; OR10G5P; LOC107984411; RNU6-256P; RNU6-874P; LOC105369561; OR8B6P; MIR125B1; RNU6-1156P; GLB1L3; BMPR1AP2; ROBO3; PKNOX2-DT; APLP2; MSANTD2; LOC101929208; LINC02731; CLMP; JAM3; OR8G1; MIR6090; ETS1-AS1; OR8G3P; LINC02712; JHY; OR4D5; LOC100419058; OR6M2P; SPATA19; LOC107984402; LINC01395; ZNF123P; OR8B10P; RNU6ATAC12P; RNU2-35P; SIAE; GSEC; RNU4-23P; OR8B3; NTM-AS1; LOC105369532; SRPRA; UBASH3B; LOC105369575; PRDM10-DT; TMEM225; LOC100507548; ZNF202; ACRV1; LOC105369572; SLC37A2; LINC02684; PKNOX2-AS1; LOC107984379; LOC107984405; OR8Q1P; MIRLET7A2; LINC02725; OR8G7P; LINC02697; OR8B12; ADAMTS15; THYN1; KIRREL3-AS2; TMEM45B; LOC105369583; PTP4A2P2; ZBTB44-DT; LOC105369543; LOC105369540; SNORD14E; ST14; ACAD8; OR10G8; DDX25; NDUFAF2P2; HEPN1; LOC107984373; PPP1R10P1; SPA17; RNU6-592P; RNU4ATAC10P; ATP5PBP5; NCAPD3; OR8B8; OR10G7; PANX3; LOC403312; RPL35AP26; SLC5A4P1; RPS27P20; RPL34P21; TRK-TTT2-1; LOC283172; BSX; OR8C1P; LOC107984413; RPL31P47; KCNJ5; RPUSD4; TIRAP-AS1; LINC02714; LOC107984350; LOC101929227; GRAMD1B; SORL1; LOC105369580; LOC105369534; DNAJB6P1; LOC107984407; VPS26B; RNU4ATAC5P; OR8B7P; LOC105369574; LOC105369577; RNU4-86P; RNA5SP352; MIR8052; RN7SKP121; ELOCP22; LOC105369545; LOC101929427; BLID; PHB1P17; ESAM; OR8D2; ST3GAL4; KIRREL3; OR10D1P; LINC02717; OR6T1; LOC105369551; VSIG2; LOC101929473; PKNOX2; B3GAT1-DT; FOXRED1; ETS1; RN7SL778P; DCPS; CHEK1; OR10D5P; TMEM218; OR8B1P; GRIK4; EI24; LOC105369571; OR8A2P; OR8B9P; KRT18P59; LOC107984404; MIR100HG; IGSF9B; SAE1P1; NFRKB; PATE4; OR8B2; OR6M1; FEZ1; FLI1; NTM; SNX19; MIR10526; LOC105369591; LOC105369579; GLB1L2; NTM-IT; OR8G5; LOC105369539; SNORD14D; OR10N1P; LOC100533644; LOC105369568; MIR3167; LINC02743; ADAMTS8; TP53AIP1; HSPA8; PRDM10; ELOBP2; LOC107984412; BAK1P2; LINC02873; SC5D; LOC105369562; GLULP3; CRTAM; LOC107984432; HMGB1P42; OR8G2P; LOC105369565; OPCML; MSANTD2-AS1; MIR100; LOC100421985; LOC102724410; LOC105369559; LOC101929653; SENCR; OR10G4; LOC112268069; See more...

Location information:

Clinical significance:

ID:: 48486606

variant

18.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC105369534; SORL1; VPS26B; TIRAP-AS1; LOC105369577; OR8A2P; RPL34P21; OR8D2; GRAMD1B; LOC105369574; ST3GAL4; RPUSD4; LINC02714; OR8B7P; TRK-TTT2-1; LOC101929473; TMEM218; KCNJ5; DNAJB6P1; RNU4ATAC5P; OR10D5P; ETS1; LOC105369571; LOC101929227; RPS27P20; DCPS; LOC100533644; NFRKB; SAE1P1; LOC105369551; KCNJ1; LOC107984407; LOC107984404; OR8D4; CCDC15; MIR4697; LOC105369533; ROBO4; OR8D1; PATE1; OR8B4; TBRG1; OR8A1; KCNJ5-AS1; LOC101929538; OR8A3P; PUS3; OR10S1; OR6M3P; RPS4XP12; CCDC15-DT; B3GAT1; TECTA; PATE2; STT3A-AS1; SF3A3P2; OR10G6; TBCEL; RN7SL167P; CDON; SNORD153; PATE3; LOC107984406; NRGN; LOC100421985; SORL1-AS1; LOC107984432; OR8G5; LOC105369576; LINC02743; MIR3167; VWA5A; LOC107984412; NTM; LOC107984409; OR8B5P; LOC105369562; GLB1L2; MIR100HG; MIR10526; LOC105369559; IGSF9B; LOC105369539; SNX19; NTM-IT; GLULP3; TP53AIP1; OR6M1; CRTAM; LOC105369579; OR8G2P; KIRREL3-AS3; OR8B2; HMGB1P42; BAK1P2; MSANTD2-AS1; OR8X1P; PRDM10; LINC02873; LOC105369575; ZBTB44; LOC112268069; GLB1L3; LOC105369532; ROBO3; OR10G5P; GSEC; SIAE; LOC105369535; LOC105369578; LOC399975; ACRV1; VSIG10L2; LOC107984411; LOC101929208; RNU6-256P; LOC105369558; JHY; LOC100421417; OR8B6P; HEPACAM; CLMP; ETS1-AS1; RNU1-21P; LINC02731; LINC02712; OR6X1; RPL34P23; STT3A; RNU6-1156P; THYN1; JAM3; MIRLET7A2; HYLS1; LINC02730; APLP2; SNORD14C; RPS26P43; OR8B12; PKNOX2-DT; MIR6090; MIR125B1; RNU6-874P; OR8F1P; BMPR1AP2; LINC02706; OR10G9; SCN3B; ESAM-AS1; ARHGAP32; MSANTD2; TIRAP; LOC107984357; LOC105369561; LOC107984374; DDX18P5; LOC105369587; NAP1L1P1; FAM118B; LINC02098; LINC02727; RNU6-321P; LINC02551; BARX2; MIR4493; DDX25; RN7SL351P; RN7SKP279; OR8G1; LOC105369544; OR10D4P; LOC403312; OR10D3; LOC107984350; HEPN1; RNU6-876P; LOC107984373; NCAPD3; ACAD8; OR10G8; BLID; LOC105369540; LOC105369580; OR8Q1P; NDUFAF2P2; OR8B8; LOC105369543; LOC105369583; MIR8052; BSX; LOC107984413; RNU4-86P; ST14; PPP1R10P1; RPL31P47; ADAMTS15; PTP4A2P2; ATP5PBP5; LOC283172; RNU6ATAC12P; RNA5SP352; TMEM225; SPA17; NTM-AS1; LINC02725; TMEM45B; OR8B10P; RNU6-592P; RNU4-23P; OR10G7; RPL35AP26; OR8G3P; LINC01395; LOC107984379; ZBTB44-DT; RNU2-35P; LOC100419058; SPATA19; ZNF123P; PKNOX2-AS1; OR8C1P; OR8B3; LOC107984405; OR8G7P; SLC37A2; LOC100507548; LOC107984402; RNU4ATAC10P; SNORD14E; PANX3; ZNF202; LOC105369572; UBASH3B; KIRREL3-AS2; PRDM10-DT; SLC5A4P1; FLI1; LINC02697; OR10D1P; OR6M2P; B3GAT1-DT; OR4D5; HSPA8; SNORD14D; SC5D; SRPRA; LOC101929427; LINC02717; MIR100; OPCML; LOC102724410; CHEK1; LOC105369565; OR8B9P; FOXRED1; LOC105369568; LOC105369545; SENCR; OR8B1P; OR10N1P; ESAM; OR6T1; LOC105369591; KIRREL3; VSIG2; ADAMTS8; OR10G4; LOC101929653; EI24; PHB1P17; RN7SL778P; ELOBP2; PATE4; FEZ1; RN7SKP121; PKNOX2; KRT18P59; GRIK4; See more...

Location information:

Clinical significance:

ID:: 48465107

variant

19.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LINC02098; LOC105369587; TIRAP; SNORD153; LOC107984357; RNU6-321P; RPS26P43; OR10D3; LOC105369544; OR10S1; OR8F1P; RN7SL351P; RNU6-876P; BARX2; CCDC15-DT; MIR4493; ESAM-AS1; BMPR1AP2; PATE2; OR8G1; OR10D4P; RN7SKP279; RPS4XP12; SNORD14C; NAP1L1P1; FAM118B; LOC107984374; LINC02727; PUS3; LINC02706; CHEK1; SCN3B; LOC107984404; OR10G9; ARHGAP32; SAE1P1; LOC105369545; OR8B1P; LINC02717; KRT18P59; LOC105369568; GRIK4; ETS1; ESAM; LOC105369551; FOXRED1; EI24; OR6T1; VSIG2; LOC105369565; TMEM218; OR8B9P; NFRKB; PATE4; ELOBP2; OR10N1P; LOC105369591; RN7SKP121; KIRREL3; LOC105369571; PKNOX2; B3GAT1-DT; SNORD14D; OR10D1P; OR8A2P; OPCML; LOC101929427; RN7SL778P; OR8D2; PHB1P17; LOC101929473; OR6M1; GLULP3; BAK1P2; MSANTD2-AS1; HMGB1P42; OR8B2; SENCR; OR10G4; OR8G2P; PRDM10; LOC101929653; CRTAM; LINC02873; ADAMTS8; LOC112268069; LINC02743; SC5D; LOC105369579; MIR3167; SORL1-AS1; HSPA8; OR8G5; LOC100421985; LOC107984432; GLB1L2; LOC107984412; VWA5A; FLI1; MIR10526; NTM; LOC105369559; IGSF9B; LOC105369562; TP53AIP1; MIR100HG; MIR100; NTM-IT; LOC102724410; SNX19; LOC105369539; OR8B8; TMEM45B; RNU6-592P; SPA17; FEZ1; ATP5PBP5; ST14; OR8C1P; OR10G7; ADAMTS15; LINC02697; SLC5A4P1; PTP4A2P2; ZBTB44-DT; LOC105369543; RPL35AP26; PPP1R10P1; PANX3; LOC107984350; DDX25; LOC283172; RPL31P47; RNU4ATAC10P; SNORD14E; NCAPD3; LOC403312; LOC107984413; ACAD8; LOC105369540; LINC02725; NDUFAF2P2; LOC105369583; HEPN1; OR10G8; LOC107984373; RNU4ATAC5P; LOC100533644; OR8Q1P; BLID; VPS26B; TRK-TTT2-1; OR10D5P; LOC105369580; LOC105369574; TIRAP-AS1; RNA5SP352; RPUSD4; LOC105369534; LOC101929227; DCPS; RNU4-86P; MIR8052; LOC107984407; RPL34P21; OR8B7P; SORL1; DNAJB6P1; ST3GAL4; RPS27P20; LOC105369577; THYN1; RNU1-21P; GRAMD1B; KCNJ5; LINC02551; CLMP; BSX; LINC02714; OR8B12; RNU6-1156P; JAM3; LOC105369575; OR6X1; MIR125B1; LINC02731; LOC101929208; LOC105369578; MSANTD2; MIR6090; OR10G5P; HYLS1; RNU6-256P; RPL34P23; LOC107984411; LINC02730; STT3A; LOC100421417; ROBO3; LOC105369558; LOC399975; PKNOX2-DT; OR8G7P; SPATA19; LOC107984402; ZNF123P; HEPACAM; SLC37A2; OR8B6P; APLP2; SIAE; LOC105369535; GLB1L3; RNU6-874P; LOC105369572; LOC107984379; KIRREL3-AS2; DDX18P5; LOC100419058; OR8G3P; UBASH3B; OR4D5; LOC105369561; LINC02712; OR8B10P; VSIG10L2; MIRLET7A2; LOC107984405; ACRV1; RNU6ATAC12P; PKNOX2-AS1; TMEM225; NTM-AS1; RNU4-23P; LINC01395; OR8B3; GSEC; LOC100507548; ETS1-AS1; SRPRA; PRDM10-DT; OR6M2P; TBCEL; KIRREL3-AS3; LOC105369532; ZNF202; OR8A3P; JHY; ZBTB44; NRGN; PATE3; LOC101929538; OR8X1P; ROBO4; RN7SL167P; TBRG1; RNU2-35P; OR10G6; LOC107984409; KCNJ5-AS1; TECTA; STT3A-AS1; LOC107984406; OR6M3P; PATE1; LOC105369533; CCDC15; SF3A3P2; OR8D4; LOC105369576; KCNJ1; OR8B4; OR8D1; B3GAT1; CDON; OR8A1; OR8B5P; MIR4697; See more...

Location information:

Clinical significance:

ID:: 49580352

variant

20.

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: OR8D2; PHB1P17; LOC101929427; OR8A2P; LOC101929473; GRIK4; ST3GAL4; FOXRED1; ETS1; OR8B9P; OR10D5P; LOC105369568; ESAM; OR6T1; LOC105369571; TMEM218; RN7SKP121; PKNOX2; RN7SL778P; PATE4; SAE1P1; EI24; CHEK1; LOC105369591; KIRREL3; LOC100533644; LOC107984404; LINC02717; NFRKB; OR8B1P; LOC105369574; LOC105369551; DCPS; B3GAT1-DT; FAM118B; OR10D1P; PATE1; LOC105369544; OR8D1; OR8D4; SCN3B; RPS4XP12; ARHGAP32; OR10S1; LOC107984357; TIRAP; OR10G9; LINC02098; SNORD153; KCNJ5-AS1; CCDC15-DT; PUS3; BARX2; RNU6-876P; PATE2; MIR4493; OR10D4P; SF3A3P2; NRGN; STT3A-AS1; OR8F1P; PATE3; OR10D3; RNU6-321P; RPS26P43; TBRG1; CCDC15; LOC105369579; RN7SKP279; OR8B5P; SORL1-AS1; TP53AIP1; OR8A1; OR8A3P; OR8B4; MSANTD2-AS1; MIR4697; LOC101929538; KIRREL3-AS3; BAK1P2; B3GAT1; OR8X1P; ZBTB44; TBCEL; LOC107984406; RN7SL167P; OR10G6; CDON; TECTA; VWA5A; LOC105369533; LOC105369576; ROBO4; LOC107984432; KCNJ1; OR6M3P; LOC107984409; OR8B10P; OR8B6P; LOC105369535; LOC399975; TMEM225; SIAE; RNU6ATAC12P; OR4D5; ETS1-AS1; LOC100419058; VSIG10L2; SPATA19; OR8G3P; HEPACAM; LINC02712; LINC01395; JHY; MIRLET7A2; RNU2-35P; OR8G7P; THYN1; LOC107984402; PKNOX2-AS1; ZNF202; LOC105369572; OR8B12; LOC107984405; SLC37A2; LOC105369575; PRDM10-DT; KIRREL3-AS2; LOC100507548; RNU4-23P; LINC02730; RNU6-256P; ACRV1; LOC101929208; ESAM-AS1; LOC105369532; UBASH3B; HYLS1; GSEC; SRPRA; MIR125B1; DDX18P5; LOC105369561; LOC105369578; LOC105369558; NAP1L1P1; LOC100421417; RNU1-21P; OR8B3; RNU6-874P; RPL34P23; OR6X1; LINC02706; LOC107984374; LINC02551; STT3A; CLMP; APLP2; LINC02727; SNORD14C; JAM3; OR10G5P; OR8G1; LOC107984411; RNU6-1156P; MIR6090; LOC107984350; GLB1L3; ROBO3; BMPR1AP2; LINC02731; OR8B7P; MSANTD2; RN7SL351P; RPUSD4; HEPN1; KCNJ5; PKNOX2-DT; LOC105369540; BLID; ACAD8; LOC105369580; RPS27P20; RNU4-86P; BSX; TIRAP-AS1; LINC02714; LOC107984413; SORL1; RPL31P47; ADAMTS15; VPS26B; TRK-TTT2-1; RPL34P21; RNA5SP352; MIR8052; GRAMD1B; LOC107984373; NTM-AS1; LOC107984407; RNU4ATAC5P; LOC105369577; RNU6-592P; OR10G8; DNAJB6P1; LOC107984379; LOC101929227; LOC105369534; NDUFAF2P2; ZBTB44-DT; OR8Q1P; PTP4A2P2; LOC105369543; ZNF123P; OR8B8; LOC105369583; OR8C1P; ST14; SLC5A4P1; PPP1R10P1; SNORD14E; LOC403312; ATP5PBP5; PANX3; TMEM45B; OR6M2P; LINC02725; NCAPD3; DDX25; RNU4ATAC10P; LINC02697; LOC105369559; LOC283172; OR10G7; LOC100421985; LOC105369539; RPL35AP26; FLI1; SNX19; OR8B2; SPA17; OR6M1; OPCML; MIR10526; MIR100; SNORD14D; LOC105369562; FEZ1; LOC102724410; OR10N1P; IGSF9B; CRTAM; LOC105369565; LOC112268069; LOC105369545; HMGB1P42; LINC02873; OR10G4; SENCR; GLULP3; PRDM10; MIR3167; LOC101929653; ADAMTS8; KRT18P59; NTM-IT; GLB1L2; ELOBP2; LOC107984412; SC5D; OR8G5; NTM; MIR100HG; OR8G2P; HSPA8; LINC02743; VSIG2; See more...

Location information:

Clinical significance:

ID:: 48468115

variant

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