SW_1322 AND estd203 - dbVar - NCBI

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1.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: LINC02315

Location information:

ID:: 11938402

variant

2.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:

Location information:

ID:: 11940711

variant

3.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: PTPRT

Location information:

ID:: 11938806

variant

4.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: LOC107986449

Location information:

ID:: 11939781

variant

5.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: SCAPER

Location information:

ID:: 11939635

variant

6.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: LINC00907

Location information:

ID:: 11940599

variant

7.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: LOC105376988

Location information:

ID:: 11940800

variant

8.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: LOC553139

Location information:

ID:: 11940492

variant

9.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:

Location information:

ID:: 11939632

variant

10.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: KIAA1217

Location information:

ID:: 11941042

variant

11.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: RPEP2; LOC105377001

Location information:

ID:: 11940558

variant

12.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: SMCO2; RARS1P1

Location information:

ID:: 11937689

variant

13.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: MLIP-IT1; LOC101927189

Location information:

ID:: 11939709

variant

14.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: MRPL49P2; LOC101929028; LOC105379297

Location information:

ID:: 11940743

variant

15.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: PRSS2; TRB; PRSS3P2; TRY7

Location information:

ID:: 11940717

variant

16.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: AMY1A; AMY1B; AMY1C; AMY2A; AMY2B; AMYP1; ACTG1P4; LOC105378878

Location information:

ID:: 11940575

variant

17.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: CFHR1; CFHR2; CFHR4; CFHR3; LOC100996886; LOC105371675

Location information:

ID:: 11937884

variant

18.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: SPATA31A6; ADGRF5P2; MEP1AP4; CNN2P4; GXYLT1P5; FKBP4P6; PTS-P1; ATP5F1AP1; ANKRD20A7P; FGF7P4; RAB28P3; LOC100420440; LOC102724818; XLOC_007697; RNU6-599P; LOC112268044; RBPJP6; LOC100419693; FAM74A7; LOC101927827; LOC112268036; RBM17P3; SNX18P5; CNTNAP3P7; CYP4F60P; FGF7P5; CNTNAP3B; CNTNAP3P8; LOC100421691; SDR42E1P2; FAM88E; RN7SL343P; See more...

Location information:

ID:: 11941058

variant

19.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: IGH; IGHVIII-67-4; IGHV8-51-1; IGHVIII-38-1; IGHVIII-22-2; IGHVII-65-1; IGHVII-53-1; IGHVII-33-1; IGHVII-28-1; IGHVII-20-1; IGHV5-51; IGHV4-61; IGHV4-39; IGHV4-4; IGHV3-64; IGHV3-60; IGHV3-53; IGHV3-49; IGHV3-37; IGHV3-33-2; IGHV3-30; IGHV3-19; IGHV3-13; IGHV3-7; IGHV2-26; IGHV1-68; IGHV1-46; IGHV1-18; GOLGA4P2; LINC00221; IGHV2-70D; LOC102724977; LOC105370700; RNA5SP389; IGHVIII-67-3; IGHVIII-25-1; IGHVIII-13-1; IGHVIII-5-1; IGHVII-60-1; IGHVII-49-1; IGHVII-43-1; IGHV7-56; IGHV7-27; IGHV5-10-1; IGHV4-55; IGHV3-66; IGHV3-63; IGHV3-50; IGHV3-47; IGHV3-41; IGHV3-36; IGHV3-30-2; IGHV3-25; IGHVIII-67-2; IGHVIII-44; IGHVIII-11-1; IGHVII-67-1; IGHVII-46-1; IGHVII-40-1; IGHVII-30-1; IGHVII-22-1; IGHV7-40; IGHV4-28; IGHV3-65; IGHV3-62; IGHV3-54; IGHV3-43; IGHV3-38; IGHV3-35; IGHV3-32; IGHV3-23; IGHV3-20; IGHV3-15; IGHV1-69; IGHV1-58; IGHV1-12; IGHV7-4-1; GOLGA4P3; HOMER2P1; LINC00226; IGHVII-30-21; LOC107984634; IGHVIV-44-1; IGHVIII-47-1; IGHVIII-26-1; IGHVIII-16-1; IGHVIII-5-2; IGHVII-62-1; IGHVII-51-2; IGHVII-44-2; IGHVII-26-2; IGHVII-15-1; IGHV7-34-1; IGHV4-59; IGHV4-34; IGHV4-30-2; IGHV3-57; IGHV3-52; IGHV3-48; IGHV3-42; IGHV3-33; IGHV3-29; IGHV3-22; IGHV3-11; IGHV3-6; IGHV1-67; IGHV1-45; IGHV1-17; SLC20A1P2; GOLGA4P1; IGHV3-21; IGHV3-16; IGHV2-5; IGHV1-24; IGHV1-14; SLC20A1P1; HOMER2P2; IGHV3-64D; See more...

Location information:

ID:: 11938414

variant

20.

Variant type:: copy number variation

Associated study:: estd203

Organism:
human

Genes(s) in region:: PDXDC2P-NPIPB14P; CLEC18A; SMG1P7; WWP2; EXOSC6; CLEC18C; NPIPB14P; PDPR; LOC400541; RPS10P24; MIR1972-2; LOC105371328; PDXDC2P; See more...

Location information:

ID:: 11939654

variant

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