"nstd125"[study] AND "copy number loss"[variant_type] - dbVar - NCBI

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Items: 5

1.

Variant type:: copy number variation

Associated study:: nstd125

Organism:
human

Genes(s) in region:: LINC02161

Location information:

ID:: 45766979

variant

2.

Variant type:: copy number variation

Associated study:: nstd125

Organism:
human

Genes(s) in region:: ADGRB3; COL9A1; COL19A1; LMBRD1; NUFIP1P1; EYS; SLC25A51P1; ADH5P4; LOC100128293; RNU7-66P; GAPDHP42; RPL37P15; LOC100420211; LOC100420940; NPM1P37; RNA5SP208; LINC02549; ADGRB3-DT; LOC102723883; LOC105377838; LOC105377839; LOC105377840; LOC105377841; LOC105377842; LOC105377843; LOC105377844; LOC105377845; LOC105377846; RNU6-280P; LOC107986540; LOC107986610; See more...

Location information:

ID:: 45766981

variant

3.

Variant type:: copy number variation

Associated study:: nstd125

Organism:
human

Genes(s) in region:: AUH; ECM2; IARS1; NFIL3; NINJ1; ROR2; OMD; OGN; SYK; SPTLC1; BICD2; DIRAS2; ASPN; NOL8; IPPK; WNK2; OR7E108P; ZNF484; CARD19; FGD3; ANKRD19P; PRSS47P; LINC00475; SUSD3; LINC01501; BEND3P2; OR7E109P; CENPP; EEF1DP2; FAM120A2P; LOC642943; SNX18P2; ALOX15P2; RPL21P82; PAICSP2; SNORA84; LOC100128076; LOC100128361; LOC100129316; LINC00484; RPL21P86; HSPE1P22; LOC100419515; LOC100420779; LOC100420896; MIR3910-1; MIR3910-2; MIR3651; LINC02937; MIR4670; MTND4P15; LINC01508; LOC101927954; LOC101927993; LOC101929748; LOC105376143; LINC02957; LOC105376146; LOC105376148; LOC105379829; RNU6-714P; MTCO3P29; MTND3P23; MTATP6P29; LOC107987094; LOC107987095; LOC112268048; See more...

Location information:

ID:: 45766984

variant

4.

Variant type:: copy number variation

Associated study:: nstd125

Organism:
human

Genes(s) in region:: BUB1; BCL2L11; MERTK; PAFAH1B1P2; ACOXL; ANAPC1; ZC3H8; TMEM87B; FBLN7; ZC3H6; ACOXL-AS1; MIR4435-2HG; RPL22P12; EEF1E1P1; RPS14P4; CENPNP2; RPL5P9; RPL34P8; LOC100418696; DBF4P2; RTRAFP1; SLC30A6P1; MIR4771-2; MIR4435-2; LOC101927283; LOC105373554; SOCAR; LOC105373559; RN7SL297P; SNORD132; NDUFB4P6; LOC107985933; See more...

Location information:

ID:: 45766958

variant

5.

Variant type:: copy number variation

Associated study:: nstd125

Organism:
human

Genes(s) in region:: ADCY1; IGFBP1; IGFBP3; EPS15P1; TTC4P1; FTLP15; SEPTIN7P2; ELK1P1; LOC730234; LOC730338; CICP20; RNU7-76P; ZNF619P1; HMGN1P19; GTF2IP13; LOC102723446; LOC105375264; LOC105375266; LOC105375267; RNU6-241P; RNU6-326P; SEPTIN14P7; LOC112267911; LOC112267918; See more...

Location information:

ID:: 45766983

variant

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"nstd125"[study] AND "copy number loss"[variant_type] (6)
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