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nsv1008496

Variant type:
copy number variation
Associated study:
nstd100
Organism:
human
Genes(s) in region:
RPS27AP6
,
CTXND2
,
LOC107985204
,
ANXA9
,
ARNT
,
LOC105371438
,
CYCSP51
,
SETDB1
,
CERS2
,
MINDY1
Location information:
ID:
17666913
variant

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