MS16801 AND nstd71 - dbVar

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nsv881222

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LOC105377513

Location information:

ID:: 9577115

variant

nsv911995

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: CEACAMP8; PSG11

Location information:

ID:: 9607888

variant

nsv881774

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LOC105379623; GUSBP3

Location information:

ID:: 9577667

variant

nsv908442

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: NSF; NSFP1; ARL17B

Location information:

ID:: 9604335

variant

nsv879310

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LOC100422402; LOC100132651; LOC728807; UGT2B17

Location information:

ID:: 9575203

variant

nsv911912

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: CEACAMP7; PSG1; PSG7; PSG6

Location information:

ID:: 9607805

variant

nsv892175

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: KDM4C; SNRPEP2; PRELID3BP11; RPL35AP20; LINC02851

Location information:

ID:: 9588068

variant

nsv871196

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: PRAMEF11; PRAMEF1; LINC01784

Location information:

ID:: 9567089

variant

nsv883932

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: HLA-K; HCG4B; HLA-A

Location information:

ID:: 9579825

variant

10.

nsv883570

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: HLA-T; HCG4P7; HLA-H

Location information:

ID:: 9579463

variant

11.

nsv883833

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: HLA-A; DDX39BP1; MCCD1P1; LOC353008

Location information:

ID:: 9579726

variant

12.

nsv880953

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LINC02064; LOC105374702; LOC100420990

Location information:

ID:: 9576846

variant

13.

nsv898668

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: RPS20P29; LOC100130582; SLC2A3; NANOGP1; SLC2A14

Location information:

ID:: 9594561

variant

14.

nsv904023

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LOC100422491; GOLGA8B; DNM1P5; GOLGA8A; MIR1233-2; FSCN1P1; HNRNPLP2

Location information:

ID:: 9599916

variant

15.

nsv911345

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: LOC105372316; BNIP3P23; LOC105372317; BNIP3P22; ZNF737; ZNF826P

Location information:

ID:: 9607238

variant

16.

nsv889043

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Location information:

ID:: 9584936

variant

17.

nsv914504

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: TOP3B; IGLVI-68; IGL; IGLV4-69; PRAMENP; IGLVI-70

Location information:

ID:: 9610397

variant

18.

nsv893230

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

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

Location information:

ID:: 9589123

variant

19.

nsv915046

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Genes(s) in region:: IGLV1-62; IGLV4-60; IGLVI-63; IGL; LOC100736408; LOC102724653; IGLV10-67; IGLVIV-65; IGLVIV-66-1; PRAMENP; ABHD17AP5; IGLVV-66; IGLV8-61; IGLVIV-64; See more...

Location information:

ID:: 9610939

variant

20.

nsv879115

Variant type:: copy number variation

Associated study:: nstd71

Organism:
human

Location information:

ID:: 9575008

variant

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MS16801 AND nstd71 (22)
dbVar
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Gorilla gorilla gorilla RefSeq Genome sequencing

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