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Items: 15

1.

nsv3878822

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LMOD3
Location information:
Clinical significance:
Pathogenic
ID:
48442177
variant
2.

nsv3916461

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377171
,
HNRNPA3P6
,
MITF
,
MIR1324
,
RPL7AP23
,
HESX1
,
LOC105377128
,
CAP1P1
,
UBL5P3
,
LOC105377174
,
PDZRN3-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479816
variant
3.

nsv3922768

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-557P
,
LOC105377160
,
OR7E121P
,
LOC105377143
,
FOXP1
,
PDZRN3
,
LOC105377146
,
LOC105377166
,
LRIG1
,
DPPA4P1
,
FRMD4B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486123
variant
8.

nsv5564432

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC137P1
,
LOC105377160
,
COX6CP6
,
HMGB1P36
,
FRMD4B
,
UBA3
,
UBE2Q2P9
,
PROK2
,
LOC105377161
,
LOC105377155
,
RBM43P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
52011855
variant
9.

nsv3885606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
SEMA3B-AS1
,
TPRG1
,
ITPR1-DT
,
LOC107986112
,
H3P12
,
NT5DC2
,
OR7E122P
,
SRGAP3
,
C3orf36
,
LOC105377018
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448961
variant
10.

nsv3889228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB4
,
LOC105374108
,
RPL6P7
,
RNY3P13
,
LINC00960
,
LOC107986110
,
TRH
,
LINC02016
,
LOC105377125
,
ZNF589
,
P2RY1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452583
variant
11.

nsv3880617

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP49
,
DLEC1
,
TFDP2
,
IGF2BP2
,
BTD
,
RBM5-AS1
,
RAB43
,
FANCD2
,
CYB561D2
,
PFN2
,
GPR149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443972
variant
13.

nsv3875054

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPLP0P8
,
EOGT
,
TMF1
,
UBA3
,
TAFA4
,
MIR3136
,
PSMC1P1
,
RNA5SP135
,
LMOD3
,
ARL6IP5
,
TAFA1
,
See more...
Location information:
Clinical significance:
not provided
ID:
48438409
variant
14.

nsv6290797

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UBA3
,
RNPC3P1
,
COX6CP6
,
HMGB1P36
,
FRMD4B
,
TMF1
,
RN7SL418P
,
EOGT
,
TAFA4
,
RBM43P1
,
LOC105377152
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53636192
variant
15.

nsv4453115

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARL6IP5
,
RBM43P1
,
LMOD3
,
TAFA4
,
TMF1
,
EOGT
,
RNA5SP135
,
UBA3
,
MIR3136
,
FRMD4B
Location information:
Clinical significance:
Uncertain significance
ID:
49618750
variant
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