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Variant : CV673256 (GRCh37/hg19 1p36.22-36.21(chr1:10246640-12841900)x1) Homo sapiens

Symbol: CV673256
Name: GRCh37/hg19 1p36.22-36.21(chr1:10246640-12841900)x1
Condition: not provided [RCV000846372]
Clinical Significance: uncertain significance
Last Evaluated: 08/31/2018
Review Status: no assertion criteria provided
Related Genes: AADACL3   AADACL4   AGTRAP   ANGPTL7   C1orf127   C1orf158   C1orf167   CASZ1   CENPS   CENPS-CORT   CLCN6   CORT   DFFA   DHRS3   DISP3   DRAXIN   EXOSC10   FBXO2   FBXO44   FBXO6   KIAA2013   KIF1B   MAD2L2   MASP2   MFN2   MIIP   MTHFR   MTOR   NPPA   NPPB   PEX14   PGD   PLOD1   PRAMEF12   SRM   TARDBP   TNFRSF1B   TNFRSF8   UBIAD1   VPS13D  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37110,246,640 - 12,841,900CLINVAR
Cytogenetic Map11p36.22-36.21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976941
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
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.