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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr10:71332204
GRCh38:
Chr10:69572448
NEUROG3not specifiedBenign/Likely benign
(Mar 29, 2016)
criteria provided, single submitter
2.
GRCh37:
Chr10:71332301
GRCh38:
Chr10:69572545
NEUROG3not specifiedBenign
(Mar 29, 2016)
criteria provided, multiple submitters, no conflicts
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