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Items: 12

1.

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
2.

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
6.

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
7.

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
8.

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
9.

nsv3871428

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377141
,
LOC105377144
,
RPL21P41
,
LOC105377128
,
SLC25A26
,
MIR4272
,
MAGI1
,
LOC105377142
,
LOC107986018
,
DPPA4P1
,
KBTBD8
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48434783
variant
10.

nsv6636503

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL482P
,
LOC105377141
,
ILF2P1
,
RPL21P41
,
LOC105377144
,
MAGI1-AS1
,
LOC107986095
,
MIR4272
,
LOC107986018
,
KBTBD8
,
DPPA4P1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54355332
variant
11.

nsv4674691

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC25A26
,
LOC105377142
,
LRIG1
,
LOC105377143
,
MAGI1-IT1
,
RNU6-787P
,
KBTBD8
,
DPPA4P1
,
RPL17P17
,
LOC105377141
,
LOC105377144
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271516
variant
12.

nsv3920642

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MAGI1-AS1
,
LOC107986095
,
RPL21P41
,
KBTBD8
,
LOC105377143
,
ILF2P1
,
RN7SL482P
,
LOC107986036
,
SLC25A26
,
LOC105377141
,
LOC105377128
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48483997
variant
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