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Items: 6

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr10:89720633-89720634
GRCh38:
Chr10:87960876-87960877
PTENPTEN hamartoma tumor syndromeLikely benign
(May 28, 2019)
criteria provided, single submitterVCV000802611
2.
GRCh37:
Chr10:89720633-89720634
GRCh38:
Chr10:87960876-87960877
PTENHereditary cancer-predisposing syndrome, not specifiedBenign/Likely benign
(Nov 25, 2014)
criteria provided, multiple submitters, no conflictsVCV000092832
3.
GRCh37:
Chr10:89720633-89720634
GRCh38:
Chr10:87960876-87960877
PTENnot specified, PTEN hamartoma tumor syndromeBenign
(May 28, 2019)
criteria provided, multiple submitters, no conflictsVCV000092831
4.
GRCh37:
Chr10:89720634-89720636
GRCh38:
Chr10:87960877-87960879
PTENPTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndromeBenign/Likely benign
(May 28, 2019)
criteria provided, multiple submitters, no conflictsVCV000229656
5.
GRCh37:
Chr10:89720634
GRCh38:
Chr10:87960877
PTENPTEN hamartoma tumor syndrome, Hereditary cancer-predisposing syndrome, not specified
Benign
(Jul 7, 2020)
criteria provided, multiple submitters, no conflictsVCV000229653
6.
GRCh37:
Chr10:89720634-89720635
GRCh38:
Chr10:87960877-87960878
PTENHereditary cancer-predisposing syndromeLikely benign
(Jul 29, 2013)
criteria provided, single submitterVCV000092833
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