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Items: 4

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr10:102005555
GRCh38:
Chr10:100245798
CWF19L1not provided, Spinocerebellar ataxia, autosomal recessive 17Pathogenic
(Dec 2, 2014)
criteria provided, single submitter
2.
GRCh37:
Chr10:102006625
GRCh38:
Chr10:100246868
CWF19L1not specifiedLikely benignno assertion criteria provided
3.
GRCh37:
Chr10:102006681
GRCh38:
Chr10:100246924
CWF19L1not specifiedLikely benignno assertion criteria provided
4.
GRCh37:
Chr10:102016044
GRCh38:
Chr10:100256287
CWF19L1not specifiedLikely benignno assertion criteria provided
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