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Items: 1 to 20 of 49

1.

nsv4455177

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLK3
,
EDC3
Location information:
Clinical significance:
Uncertain significance
ID:
49620812
variant
2.

nsv3916249

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H3P40
,
EEF1B2P1
,
MTHFS
,
HIGD2B
,
MIR4715
,
CPEB1-AS1
,
LOC440311
,
DNAAF4-CCPG1
,
EPB42
,
PWAR4
,
LOC101929129
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479604
variant
3.

nsv3919468

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-18P
,
GOLGA8K
,
LOC105370861
,
DNAAF4
,
TMOD3
,
HSP90B2P
,
TMED3
,
LOC105370752
,
ADPGK
,
MIR184
,
RNA5SP392
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482823
variant
4.

nsv3913942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNX33
,
RNA5SP399
,
RN7SL510P
,
HMG20A
,
DNAJA4-DT
,
SALRNA3
,
LOC105370891
,
INSYN1
,
TMEM202-AS1
,
DNM1P49
,
LOC101929439
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477297
variant
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