GRCh37/hg19 Xp22.2(chrX:11770846-12680420)x3 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000684275.1
Allele description [Variation Report for GRCh37/hg19 Xp22.2(chrX:11770846-12680420)x3]
GRCh37/hg19 Xp22.2(chrX:11770846-12680420)x3
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
Homo sapiens chromosome Y, whole genome shotgun sequence
Homo sapiens chromosome Y, whole genome shotgun sequencegi|74273658|gnl|WGS:AADB|chry|gb|CM 5.1|Nucleotide
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Last Updated: Apr 23, 2022