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Items: 10

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr3:49059205
GRCh38:
Chr3:49021772
NDUFAF3not specifiedLikely benign
(Jan 19, 2016)
criteria provided, single submitter
2.
GRCh37:
Chr3:49059764
GRCh38:
Chr3:49022331
NDUFAF3not specifiedBenign
(Apr 3, 2014)
criteria provided, single submitter
3.
GRCh37:
Chr3:49059894
GRCh38:
Chr3:49022461
NDUFAF3not specifiedUncertain significance
(Sep 4, 2014)
criteria provided, single submitter
4.
GRCh37:
Chr3:49059911
GRCh38:
Chr3:49022478
NDUFAF3not specifiedLikely benign
(May 23, 2017)
criteria provided, single submitter
5.
GRCh37:
Chr3:49059956
GRCh38:
Chr3:49022523
NDUFAF3not specifiedBenign
(Jul 1, 2015)
criteria provided, single submitter
6.
GRCh37:
Chr3:49060139
GRCh38:
Chr3:49022706
NDUFAF3not specifiedUncertain significance
(Jan 18, 2014)
criteria provided, single submitter
7.
GRCh37:
Chr3:49060420
GRCh38:
Chr3:49022987
NDUFAF3not specifiedLikely benign
(Dec 21, 2016)
criteria provided, single submitter
8.
GRCh37:
Chr3:49060497
GRCh38:
Chr3:49023064
NDUFAF3not providedLikely pathogenic
(Apr 18, 2016)
criteria provided, single submitter
9.
GRCh37:
Chr3:49060539-49060540
GRCh38:
Chr3:49023106-49023107
NDUFAF3not providedLikely pathogenic
(Feb 9, 2016)
criteria provided, single submitter
10.
GRCh37:
Chr3:37028313-49929220
See casesLikely pathogenic
(Jan 20, 2016)
criteria provided, single submitter
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