nsv3924800 - dbVar - NCBI

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Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: CDR2; UQCRC2; EEF2K; POLR3E; VWA3A; PDZD9; ABCA3P1; NPIPB4; CDR2-DT; MOSMO; TRL-TAG3-1; TRL-AAG2-4; SDR42E2; LOC100420536; LOC100420644; SMG1P4; LOC105371129; MFSD13B; LOC112268174; See more...

Location information:

Clinical significance:
Uncertain significance; Pathogenic/Likely pathogenic

ID:: 48488155

variant

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ClinVar
Clinical reports for this variation
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
Taxonomy
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