Center for Genetic Medicine Research
(Children's National Medical Center)
General information
Center for Genetic Medicine Research
Children's National Medical Center
111 Michigan Ave NW
Washington
District of Columbia
United States - 20010
Organization ID: 505157
Assertion criteria
Level: Assertion criteria provided
Summary of submissions to ClinVar
Total submissions: 74
Gene
Gene | Submissions | Last Updated |
---|
ACTA1 | 3 | Jan 25, 2016 |
ANO5 | 2 | Jan 25, 2016 |
CAPN3 | 1 | Jan 25, 2016 |
CAV3 | 2 | Jan 25, 2016 |
COL6A1 | 2 | Jan 25, 2016 |
COL6A2 | 4 | Jan 25, 2016 |
COL6A3 | 4 | Jan 25, 2016 |
DES | 2 | Jan 25, 2016 |
DMD | 2 | Jan 25, 2016 |
DNM2 | 2 | Jan 25, 2016 |
DYNC1H1 | 1 | Jul 15, 2014 |
DYSF | 3 | Jan 25, 2016 |
FKRP | 2 | Jan 25, 2016 |
ITGA7 | 2 | Jan 25, 2016 |
LAMA2 | 4 | Jan 25, 2016 |
LMNA | 2 | Jan 25, 2016 |
LOC126806426 | 1 | Jan 25, 2016 |
LOC126806427 | 1 | Jan 25, 2016 |
LOC126806429 | 1 | Jan 25, 2016 |
LOC126862115 | 1 | Jan 25, 2016 |
LOC129935182 | 1 | Jan 25, 2016 |
MYH7 | 2 | Jan 25, 2016 |
MYOT | 1 | Jan 25, 2016 |
NEB | 3 | Jan 25, 2016 |
OXTR | 1 | Jan 25, 2016 |
PKD2L2-DT | 1 | Jan 25, 2016 |
POMT2 | 3 | Jan 25, 2016 |
RIF1 | 1 | Jan 25, 2016 |
RYR1 | 5 | Jan 25, 2016 |
SELENON | 1 | Jan 25, 2016 |
SSUH2 | 1 | Jan 25, 2016 |
TPM2 | 1 | Jan 25, 2016 |
TPM3 | 1 | Jan 25, 2016 |
TTN | 19 | Jan 25, 2016 |
TTN-AS1 | 13 | Jan 25, 2016 |
Condition
Name | Submissions | Last Updated | Actin accumulation myopathy | 1 | Jan 25, 2016 |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | 1 | Jul 15, 2014 |
Autosomal recessive limb-girdle muscular dystrophy type 2A | 1 | Jan 25, 2016 |
Autosomal recessive limb-girdle muscular dystrophy type 2B | 2 | Jan 25, 2016 |
Autosomal recessive limb-girdle muscular dystrophy type 2I | 1 | Jan 25, 2016 |
Autosomal recessive limb-girdle muscular dystrophy type 2J | 1 | Jan 25, 2016 |
Autosomal recessive limb-girdle muscular dystrophy type 2L | 2 | Jan 25, 2016 |
Autosomal recessive limb-girdle muscular dystrophy type 2N | 1 | Jan 25, 2016 |
Bethlem myopathy 1A | 2 | Jan 25, 2016 |
Central core myopathy | 4 | Jan 25, 2016 |
Congenital muscular dystrophy | 3 | Jan 25, 2016 |
Congenital muscular dystrophy with rigid spine | 1 | Jan 25, 2016 |
Congenital myopathy | 2 | Jan 25, 2016 |
Congenital myopathy 23 | 1 | Jan 25, 2016 |
Congenital myopathy 4B, autosomal recessive | 1 | Jan 25, 2016 |
Desmin-related myofibrillar myopathy | 2 | Jan 25, 2016 |
Duchenne muscular dystrophy | 1 | Jan 25, 2016 |
Emery-Dreifuss muscular dystrophy 2, autosomal dominant | 1 | Jan 25, 2016 |
Merosin deficient congenital muscular dystrophy | 1 | Jan 25, 2016 |
Miyoshi muscular dystrophy 1 | 1 | Jan 25, 2016 |
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2 | 1 | Jan 25, 2016 |
Nemaline myopathy 2 | 1 | Jan 25, 2016 |
Rippling muscle disease 2 | 1 | Jan 25, 2016 |
not specified | 41 | Jan 25, 2016 |