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Variant : CV74785 (GRCh38/hg38 1q44(chr1:244498870-248918610)x1) Homo sapiens

Symbol: CV74785
Name: GRCh38/hg38 1q44(chr1:244498870-248918610)x1
Condition: See cases [RCV000054064]
Clinical Significance: pathogenic
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: AHCTF1   C1orf229   CATSPERE   CNST   COX20   DESI2   EFCAB2   GCSAML   GCSAML-AS1   HNRNPU   KIF26B   KIF26B-AS1   LINC01341   LINC01743   LYPD8   MIR3124   MIR3916   NLRP3   OR11L1   OR13G1   OR14A16   OR14A2   OR14C36   OR14I1   OR14K1   OR1C1   OR2AJ1   OR2AK2   OR2B11   OR2C3   OR2G2   OR2G3   OR2G6   OR2L13   OR2L2   OR2L3   OR2L5   OR2L8   OR2M2   OR2M3   OR2M4   OR2M5   OR2M7   OR2T1   OR2T10   OR2T11   OR2T12   OR2T2   OR2T27   OR2T29   OR2T3   OR2T33   OR2T34   OR2T35   OR2T4   OR2T5   OR2T6   OR2T7   OR2T8   OR2W3   OR2W5   OR6F1   PGBD2   SCCPDH   SH3BP5L   SMYD3   SMYD3-AS1   SNORA100   TFB2M   TRE-CTC2-1   TRIM58   TRL-CAA4-1   VN1R5   ZNF124   ZNF496   ZNF669   ZNF670   ZNF670-ZNF695   ZNF672   ZNF692   ZNF695  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000001.11:g.(?_244498870)_(248918610_?)del
Human AssemblyChrPosition (strand)Source
GRCh381244,498,870 - 248,918,610CLINVAR
GRCh371244,662,172 - 249,212,809CLINVAR
Build 361242,728,795 - 247,179,432CLINVAR
Cytogenetic Map11q44CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 8620977
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE


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