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Items: 11

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr12:98909635
GRCh38:
Chr12:98515857
TMPO, TMPO-AS1not specifiedLikely benign
(Jun 13, 2017)
criteria provided, single submitter
2.
GRCh37:
Chr12:98909732
GRCh38:
Chr12:98515954
TMPO, TMPO-AS1Loeys-Dietz syndrome 2, not specifiedBenign
(May 7, 2017)
criteria provided, multiple submitters, no conflicts
3.
GRCh37:
Chr12:98909753
GRCh38:
Chr12:98515975
TMPO, TMPO-AS1not specifiedLikely benign
(Mar 14, 2017)
criteria provided, single submitter
4.
GRCh37:
Chr12:98909760
GRCh38:
Chr12:98515982
TMPO, TMPO-AS1not specifiedUncertain significance
(Jul 19, 2017)
criteria provided, single submitter
5.
GRCh37:
Chr12:98909798
GRCh38:
Chr12:98516020
TMPO, TMPO-AS1not specifiedLikely benign
(Sep 7, 2017)
criteria provided, single submitter
6.
GRCh37:
Chr12:98909832
GRCh38:
Chr12:98516054
TMPO, TMPO-AS1not specifiedUncertain significance
(Apr 3, 2017)
criteria provided, single submitter
7.
GRCh37:
Chr12:98909873
GRCh38:
Chr12:98516095
TMPO, TMPO-AS1not specifiedLikely benign
(Dec 26, 2017)
criteria provided, single submitter
8.
GRCh37:
Chr12:98909877
GRCh38:
Chr12:98516099
TMPO, TMPO-AS1not specifiedUncertain significance
(Jan 9, 2014)
criteria provided, single submitter
9.
GRCh37:
Chr12:98909894
GRCh38:
Chr12:98516116
TMPO, TMPO-AS1not specifiedLikely benign
(Sep 7, 2016)
criteria provided, single submitter
10.
GRCh37:
Chr12:98909897
GRCh38:
Chr12:98516119
TMPO, TMPO-AS1not specified, Cardiovascular phenotype, Dilated Cardiomyopathy, Dominant
Conflicting interpretations of pathogenicity
(Nov 2, 2016)
criteria provided, conflicting interpretations
11.
GRCh37:
Chr12:98909908
GRCh38:
Chr12:98516130
TMPO, TMPO-AS1not specifiedUncertain significance
(Dec 19, 2016)
criteria provided, single submitter
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