dnaaf4[All Fields] AND 1[has_clinical] - dbVar

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nsv7094299

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 55274488

variant

nsv4768348

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; DNAAF4

Location information:

Clinical significance:

ID:: 50453153

variant

nsv3871988

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; DNAAF4

Location information:

Clinical significance:

ID:: 48435343

variant

nsv7094389

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 55274578

variant

nsv4453901

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 49619536

variant

nsv7094390

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 55274579

variant

nsv5672586

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 52233721

variant

nsv3880335

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 48443690

variant

nsv7099025

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 55279751

variant

10.

nsv3887587

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; DNAAF4

Location information:

Clinical significance:

ID:: 48450942

variant

11.

nsv5674305

Variant type:: insertion

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4; DNAAF4-CCPG1

Location information:

Clinical significance:

ID:: 52235440

variant

12.

nsv4681965

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; PIERCE2; DNAAF4; LOC100420711

Location information:

Clinical significance:

ID:: 50284645

variant

13.

nsv4716478

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; DNAAF4; LOC100420711

Location information:

Clinical significance:

ID:: 50356585

variant

14.

nsv3899193

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; CCPG1; MIR628

Location information:

Clinical significance:

ID:: 48462548

variant

15.

nsv4729716

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PRTG; DNAAF4; PYGO1

Location information:

Clinical significance:

ID:: 50373353

variant

16.

nsv3914320

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CCPG1; DNAAF4-CCPG1; LOC100420711; PIERCE2; DNAAF4

Location information:

Clinical significance:

ID:: 48477675

variant

17.

nsv3909042

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LOC100420711; DNAAF4; DNAAF4-CCPG1; PIERCE2

Location information:

Clinical significance:

ID:: 48472397

variant

18.

nsv6637239

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: DNAAF4-CCPG1; CCPG1; PIGB; PIGBOS1

Location information:

Clinical significance:

ID:: 54356068

variant

19.

nsv7094725

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PIGBOS1; DNAAF4-CCPG1; CCPG1; PIGB

Location information:

Clinical significance:

ID:: 55274914

variant

20.

nsv5380921

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: PIERCE2; DNAAF4; DNAAF4-CCPG1; LOC100420711

Location information:

Clinical significance:

ID:: 51636178

variant

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