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Items: 1 to 20 of 26

1.

nsv3880764

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PPARG
Location information:
Clinical significance:
Benign
ID:
48444119
variant
2.

nsv3875306

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PPARG
Location information:
Clinical significance:
Benign
ID:
48438661
variant
3.

nsv3905232

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E122P
,
SRGAP3
,
RPL21P17
,
SRGAP3-AS4
,
ARPC4
,
MARK2P20
,
ITPR1-DT
,
EDEM1
,
RPSAP32
,
CYCSP12
,
MRPS36P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468587
variant
4.

nsv3885461

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARK2P14
,
RN7SL147P
,
LMCD1
,
GHRL
,
CIDECP1
,
VGLL4
,
LMCD1-AS1
,
LOC107986040
,
RNA5SP123
,
ATG7
,
EGOT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448816
variant
6.

nsv7148081

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC6A1-AS1
,
LOC101927467
,
TATDN2
,
ATP2B2-IT2
,
LOC105376951
,
ATP2B2
,
CYCSP12
,
LINC00852
,
MIR378B
,
SLC6A1
,
VHL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55377997
variant
7.

nsv6291061

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TAMM41
,
ACTG1P12
,
SLC6A1-AS1
,
PPARG
,
LOC101927467
,
SYN2
,
LOC105376951
,
CYCSP12
,
CHCHD4P4
,
NUP210P2
,
MARK2P20
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53636456
variant
8.

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
9.

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
10.

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
11.

nsv3905127

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02022
,
RPL23AP43
,
MYRIP
,
LINC01981
,
TATDN2
,
NUP210
,
NPM1P23
,
LOC102723596
,
LOC107986011
,
PLCL2
,
LMCD1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468482
variant
12.

nsv3876280

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OXTR
,
LOC105376944
,
LOC107986058
,
XPC
,
RPL31P19
,
TRNT1
,
GADL1
,
RNU6-822P
,
DUSP5P2
,
LOC105376941
,
RNU6-815P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439635
variant
13.

nsv3892895

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL34P11
,
RNU1-96P
,
VN1R21P
,
LINC02022
,
TOP2B
,
NGLY1
,
LOC105376926
,
CNTN4
,
PP2D1
,
DCLK3
,
GALNT15
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456250
variant
14.

nsv3878718

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRRC3B
,
CCR4
,
RNU6-342P
,
XPC
,
SAP18P3
,
MKRN2
,
LOC101927829
,
COLQ
,
MIR4442
,
LOC100293612
,
RNU6-815P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48442073
variant
15.

nsv3875913

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS27P11
,
LOC107986059
,
RARB
,
THAP5P2
,
COL6A4P1
,
FGD5P1
,
LINC00312
,
RN7SL120P
,
PRRT3
,
RBMS3-AS3
,
LOC102723512
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439268
variant
16.

nsv3901059

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL32
,
RPL15
,
RPUSD3
,
LOC107986070
,
TBC1D5
,
HMGB1P5
,
CRIP1P2
,
TPRXL
,
LOC105377002
,
LOC105377005
,
ZNF385D-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464414
variant
17.

nsv3923656

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL4P
,
TOP2B
,
LOC107986065
,
VENTXP4
,
H3P10
,
NGLY1
,
RNA5SP128
,
ZCWPW2
,
SNORA93
,
LOC107986042
,
RPL31P20
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487011
variant
18.

nsv3875223

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
XPC-AS1
,
LOC101927394
,
MIR563
,
TSEN2
,
SATB1-AS1
,
TRC-GCA25-1
,
HDAC11
,
KAT2B
,
CRB3P1
,
ATG7
,
EGOT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438578
variant
19.

nsv3904668

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
C3orf20
,
LOC107986059
,
LOC101927647
,
RNU6-1194P
,
THAP5P2
,
SETD5
,
ITPR1
,
SATB1
,
IQSEC1
,
LOC107986065
,
RPL23AP39
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468023
variant
20.

nsv3907461

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TAMM41
,
CYCSP11
,
TRC-GCA25-1
,
LINC01267
,
MIR563
,
GRIP2
,
RNU6-454P
,
LOC107986066
,
DNAJC19P4
,
LOC105376958
,
TSEN2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470816
variant
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