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Items: 4

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr16:15185186
GRCh38:
Chr16:15091329
PDXDC1, RRN3D80Nnot providedBenign
(Dec 31, 2019)
criteria provided, single submitterVCV000775037
2.
GRCh37:
Chr16:15188028
GRCh38:
Chr16:15094171
PDXDC1, RRN3not providedLikely benign
(Aug 16, 2018)
criteria provided, single submitterVCV000728888
3.
GRCh37:
Chr16:15048643-15123173
PDXDC1not providedBenign
(Mar 2, 2012)
no assertion criteria providedVCV000602431
4.
GRCh37:
Chr16:15048781-15073773
GRCh38:
Chr16:14954924-14979916
PDXDC1See casesBenign
(Mar 8, 2011)
no assertion criteria providedVCV000147050
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