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Variant : CV437712 (NC_000023.10:g.(28450110_28771544)_(31838019_32614088)del) Homo sapiens

Symbol: CV437712
Name: NC_000023.10:g.(28450110_28771544)_(31838019_32614088)del
Condition: Congenital adrenal hypoplasia, X-linked [RCV000512729]
Clinical Significance: pathogenic
Last Evaluated: 10/16/2017
Review Status: criteria provided, single submitter
Related Genes: CXorf21   DMD   FTHL17   GK   IL1RAPL1   MAGEB1   MAGEB2   MAGEB3   MAGEB4   MIR3915   MIR4666B   MIR6134   NR0B1   TAB3   TAB3-AS1  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.(28450110_28771544)_(31838019_32614088)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X28,753,427 - 31,819,902CLINVAR
GRCh37X28,771,544 - 31,838,019CLINVAR
Cytogenetic MapXXp21.3-21.1CLINVAR
Trait Synonyms: ADRENAL HYPOPLASIA, CONGENITAL, WITH HYPOGONADOTROPIC HYPOGONADISM; Isolated X-Linked Adrenal Hypoplasia Congenita



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445685
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.