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Items: 5

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr11:125871721
GRCh38:
Chr11:126001826
CDONnot provided, HoloprosencephalyLikely benign
(May 9, 2017)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr11:125853944
GRCh38:
Chr11:125984049
CDONHoloprosencephaly 11Pathogenic
(Aug 12, 2011)
no assertion criteria provided
3.
GRCh37:
Chr11:125864942
GRCh38:
Chr11:125995047
CDONHoloprosencephaly 11Pathogenic
(Aug 12, 2011)
no assertion criteria provided
4.
GRCh37:
Chr11:125867125
GRCh38:
Chr11:125997230
CDONHoloprosencephaly 11Pathogenic
(Aug 12, 2011)
no assertion criteria provided
5.
GRCh37:
Chr11:125871707
GRCh38:
Chr11:126001812
CDONHoloprosencephaly 11, not providedPathogenic/Likely pathogenic
(Nov 3, 2016)
criteria provided, single submitter
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