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Items: 1 to 100 of 328

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MT-ATP6, MT-ATP8
+20 more
Deletion
Macrocytic dyserythropoietic anemia
+1 more
GLikely pathogenic
MT-ATP6, MT-ATP8
+18 more
Deletion
Mitochondrial disease
GPathogenic
MT-ND5, MT-ND6
+12 more
Deletion
Mitochondrial disease
GPathogenic
MT-ND5, MT-ND6
+9 more
Deletion
Mitochondrial disease
GPathogenic
MT-TL2, MT-TS2
+6 more
Deletion
not provided
GPathogenic
MT-CYB, MT-ND4
+6 more
Deletion
Pearson syndrome
GPathogenic
MT-TE, MT-CYB
+6 more
Deletion
Mitochondrial disease
GPathogenic
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Autosomal recessive spinocerebellar ataxia 20
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Microsatellite
Mitochondrial disease
GLikely pathogenic
MT-CYB
Single nucleotide variant
Familial cancer of breast
GBenign
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
+1 more
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
MT-CYB associated Exercise intolerance
+2 more
GPathogenic/Likely pathogenic
MT-CYB
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-CYB
Single nucleotide variant
Mitochondrial cytopathy
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
Gnot provided
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Familial cancer of breast
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Familial cancer of breast
GBenign
MT-CYB
Single nucleotide variant
not provided
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
+1 more
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
not provided
+1 more
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Familial cancer of breast
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Familial cancer of breast
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Familial cancer of breast
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
not specified
GBenign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-CYB
Single nucleotide variant
Ovarian neoplasm
GLikely benign
MT-CYB
Single nucleotide variant
Leigh syndrome
GUncertain significance
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