GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 22, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000846016.2
Allele description [Variation Report for GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1]
GRCh37/hg19 10p12.1(chr10:25133682-25277446)x1
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
HCMV_Congenital_Collection
HCMV_Congenital_CollectionNGS data for a collection of congenital samples of patients infected with HCMVBioProject
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Last Updated: Dec 11, 2022