sample57 AND nstd145 - dbVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 20 of 34

<< First< Prev

Page of 2

Next >Last >>

nsv3117809

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: SIRPB1

Location information:

ID:: 46614969

variant

nsv3110960

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: UGT2B17

Location information:

ID:: 46608120

variant

nsv3114057

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: SIGLEC14

Location information:

ID:: 46611217

variant

nsv3114178

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: MLIP

Location information:

ID:: 46611338

variant

nsv3116724

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: LOC107984964

Location information:

ID:: 46613884

variant

nsv3115553

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: CACNG2-DT

Location information:

ID:: 46612713

variant

nsv3112483

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: LOC105376360

Location information:

ID:: 46609643

variant

nsv3115311

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: P3H2

Location information:

ID:: 46612471

variant

nsv3115215

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: TENM2

Location information:

ID:: 46612375

variant

10.

nsv3114933

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: ZNF229

Location information:

ID:: 46612093

variant

11.

nsv3111015

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: CNTNAP2

Location information:

ID:: 46608175

variant

12.

nsv3117482

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:

Location information:

ID:: 46614642

variant

13.

nsv3114312

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: LOC105374814

Location information:

ID:: 46611472

variant

14.

nsv3110522

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: HSF2BP; RPL31P1

Location information:

ID:: 46607682

variant

15.

nsv3112671

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: KIF26B; DNAJC19P8

Location information:

ID:: 46609831

variant

16.

nsv3115370

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Genes(s) in region:: KRTAP9-11P; KRTAP9-7; KRTAP9-6

Location information:

ID:: 46612530

variant

17.

nsv3110903

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Location information:

ID:: 46608063

variant

18.

nsv3116586

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Location information:

ID:: 46613746

variant

19.

nsv3115280

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Location information:

ID:: 46612440

variant

20.

nsv3111954

Variant type:: copy number variation

Associated study:: nstd145

Organism:
human

Location information:

ID:: 46609114

variant

<< First< Prev

Page of 2

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

sample57 AND nstd145 (35)
dbVar
Assembly for Nucleotide (Select 2593269337) (1)
Assembly
STK32C serine/threonine kinase 32C [Homo sapiens]
STK32C serine/threonine kinase 32C [Homo sapiens]
Gene ID:282974

Gene
Gene Links for Nucleotide (Select 1519314141) (1)
Gene
SRA Links for BioSample (Select 5817825) (62)
SRA

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)

Support Center

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 34

Send to:

Supplemental Content

Find related data

Search details

Recent activity