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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr4:57522097
GRCh38:
Chr4:56655931
HOPXnot specifiedUncertain significance
(Jul 7, 2010)
criteria provided, single submitter
2.
GRCh37:
Chr4:57522134
GRCh38:
Chr4:56655968
HOPXCardiomyopathy, not specifiedLikely benign
(Aug 18, 2011)
criteria provided, single submitter
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