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Variant : CV674222 (GRCh37/hg19 Xq13.3-21.31(chrX:74667077-90312981)x1) Homo sapiens

Symbol: CV674222
Name: GRCh37/hg19 Xq13.3-21.31(chrX:74667077-90312981)x1
Condition: not provided [RCV000847338]
Clinical Significance: pathogenic
Last Evaluated: 09/14/2017
Review Status: no assertion criteria provided
Related Genes: APOOL   ATP7A   ATRX   BRWD3   CHM   COX7B   CPXCR1   CYLC1   CYSLTR1   DACH2   FGF16   GPR174   HDX   HMGN5   ITM2A   KLHL4   LPAR4   MAGEE1   MAGEE2   MAGT1   P2RY10   PBDC1   PGAM4   PGK1   POF1B   POU3F4   RPS6KA6   RTL3   SATL1   SH3BGRL   TAF9B   TBX22   TENT5D   TGIF2LX   ZDHHC15   ZNF711  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X74,667,077 - 90,312,981CLINVAR
Cytogenetic MapXXq13.3-21.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976375
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-24
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.