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Items: 4

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr11:66468469
GRCh38:
Chr11:66700998
SPTBN2not specified, Spinocerebellar Ataxia, DominantBenign/Likely benign
(Jun 14, 2016)
criteria provided, single submitter
2.
GRCh37:
Chr11:66478083
GRCh38:
Chr11:66710612
SPTBN2not specifiedUncertain significance
(Oct 28, 2014)
criteria provided, single submitter
3.
GRCh37:
Chr11:66481633
GRCh38:
Chr11:66714162
SPTBN2not specified, Spinocerebellar Ataxia, DominantLikely benign
(Jun 14, 2016)
criteria provided, single submitter
4.
GRCh37:
Chr11:66483429
GRCh38:
Chr11:66715958
SPTBN2AtaxiaLikely pathogenic
(Feb 12, 2015)
criteria provided, single submitter
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