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Items: 2

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr7:130038773
GRCh38:
Chr7:130398932
CEP41not specified, not providedUncertain significance
(May 20, 2016)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr7:130040587
GRCh38:
Chr7:130400746
CEP41not specified, not providedBenign/Likely benign
(Mar 10, 2017)
criteria provided, multiple submitters, no conflicts
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