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Variant : CV435818 (GRCh37/hg19 Yp11.2(chrY:6118157-9180657)x2) Homo sapiens

Symbol: CV435818
Name: GRCh37/hg19 Yp11.2(chrY:6118157-9180657)x2
Condition: See cases [RCV000511721]
Clinical Significance: likely benign
Last Evaluated: 10/21/2014
Review Status: no assertion criteria provided
Related Genes: AMELY   FAM197Y9   TBL1Y   TSPY4   TTTY11   TTTY12   TTTY13B   TTTY16   TTTY18   TTTY19   TTTY1B   TTTY20   TTTY21B   TTTY2B   TTTY7   TTTY8B  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37Y6,118,157 - 9,180,657CLINVAR
Cytogenetic MapYYp11.2CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13444690
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-05-26
Status: ACTIVE


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