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Items: 4

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr8:74888616
GRCh38:
Chr8:73976381
TMEM70not specified, Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear TypeBenign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
2.
GRCh37:
Chr8:74893419
GRCh38:
Chr8:73981184
TMEM70not specified, Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear TypeBenign/Likely benign
(Jun 14, 2016)
criteria provided, multiple submitters, no conflicts
3.
GRCh37:
Chr8:74893821
GRCh38:
Chr8:73981586
TMEM70not specified, Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear TypeBenign/Likely benign
(Jun 14, 2016)
criteria provided, single submitter
4.
GRCh37:
Chr8:74893850
GRCh38:
Chr8:73981615
TMEM70not specified, Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear TypeBenign/Likely benign
(Jun 14, 2016)
criteria provided, single submitter
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