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Items: 4

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
ChrX:24073761
GRCh38:
ChrX:24055644
EIF2S3not specifiedLikely benignno assertion criteria provided
2.
GRCh37:
ChrX:24073803
GRCh38:
ChrX:24055686
EIF2S3not specifiedLikely benign
(Jun 15, 2015)
criteria provided, single submitter
3.
GRCh37:
ChrX:24075862
GRCh38:
ChrX:24057745
EIF2S3not specifiedLikely benignno assertion criteria provided
4.
GRCh37:
ChrX:24091291
GRCh38:
ChrX:24073174
EIF2S3not specifiedLikely benignno assertion criteria provided
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