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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr20:13765897
GRCh38:
Chr20:13785251
NDUFAF5not specifiedConflicting interpretations of pathogenicity
(Jun 27, 2014)
criteria provided, conflicting interpretations
2.
GRCh37:
Chr20:13782194
GRCh38:
Chr20:13801548
NDUFAF5not specifiedBenign/Likely benign
(May 3, 2012)
criteria provided, single submitter
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