GRCh38/hg38 7q35(chr7:143735880-144155736)x3 AND See cases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 21, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000139760.5
Allele description [Variation Report for GRCh38/hg38 7q35(chr7:143735880-144155736)x3]
GRCh38/hg38 7q35(chr7:143735880-144155736)x3
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
1p36 Deletion Syndrome – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY - GeneRe...
1p36 Deletion Syndrome – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY - GeneReviews®
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PREDICTED: Homo sapiens homologous recombination factor with OB-fold (HROB), tra...
PREDICTED: Homo sapiens homologous recombination factor with OB-fold (HROB), transcript variant X20, mRNAgi|2462557364|ref|XM_054317110.1|Nucleotide
-
PREDICTED: Homo sapiens neuronal PAS domain protein 4 (NPAS4), transcript varian...
PREDICTED: Homo sapiens neuronal PAS domain protein 4 (NPAS4), transcript variant X3, mRNAgi|2462524466|ref|XM_054368418.1|Nucleotide
-
Homo sapiens mRNA; cDNA DKFZp686J06205 (from clone DKFZp686J06205)
Homo sapiens mRNA; cDNA DKFZp686J06205 (from clone DKFZp686J06205)gi|34365090|emb|BX640825.1|Nucleotide
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Last Updated: May 7, 2024