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Items: 19

1.

nsv3882713

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RIOX2
,
GABRR3
,
CRYBG3
Location information:
Clinical significance:
Uncertain significance
ID:
48446068
variant
2.

nsv3918176

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373994
,
RIOX2
,
GABRR3
,
CRYBG3
Location information:
Clinical significance:
Uncertain significance
ID:
48481531
variant
3.

nsv7148201

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NECTIN3
,
H2BP3
,
PLCXD2
,
SEC22A
,
LNP1
,
SSX2IPP1
,
CMSS1
,
INAVAP1
,
GUCA1C
,
RDUR
,
CCDC80
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378117
variant
4.

nsv3918661

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTCO2P29
,
GAP43
,
LOC105374010
,
DHFR2
,
SSX2IPP1
,
NIT2
,
RPL7AP11
,
GUCA1C
,
SEC22A
,
LNP1
,
HNRNPKP4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482016
variant
5.

nsv3917160

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATP6V1A
,
RPS10P4
,
HP09053
,
OR5H8
,
TIGIT
,
RPS18P5
,
TUBBP11
,
OR7E100P
,
LINC00488
,
MIR4446
,
NECTIN3-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480515
variant
6.

nsv3910775

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZBTB11-AS1
,
RABGGTBP1
,
LINC01215
,
NECTIN3-AS1
,
RN7SL767P
,
LOC105374029
,
FAM136CP
,
OR5K1
,
OR5H3P
,
LINC00636
,
CD200R1L
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474130
variant
7.

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
8.

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
9.

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
10.

nsv3922717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E53P
,
HSPA8P9
,
H3P12
,
RPS3AP14
,
OR5AC4P
,
RAD51AP1P1
,
ITGB5
,
ZBTB20-AS1
,
RLIG1P2
,
COL6A6
,
CHST2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486072
variant
12.

nsv6314751

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AKR1B1P2
,
COL8A1
,
CPOX
,
EPHA3
,
GBE1
,
GPR15
,
HTR1F
,
CNTN3
,
POU1F1
,
PROS1
,
PROS2P
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
53678774
variant
14.

nsv3874747

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373998
,
OR5H14
,
LOC101929320
,
OR5H6
,
LOC107986103
,
POU5F1P7
,
OR5K3
,
OR5H4P
,
LOC105373999
,
OR5H15
,
LOC101929298
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48438102
variant
15.

nsv4673879

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RIOX2
,
OR5BM1P
,
OR5H1
,
LOC105373994
,
ARL6
,
LOC105373997
,
OR5H7P
,
OR5H5P
,
OR5H3P
,
OR5H4P
,
POU5F1P7
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50270704
variant
16.

nsv6636842

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373997
,
LOC105374000
,
OR5H7P
,
ARL6
,
LOC105373994
,
OR5K4
,
OR5K1
,
OR5H8
,
OR5H5P
,
OR5H3P
,
OR5H14
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54355671
variant
17.

nsv4674762

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR5H4P
,
LOC105373999
,
GABRR3
,
OR5K3
,
OR5K2
,
LOC105373996
,
RIOX2
,
OR5H1
,
LOC105373997
,
OR5BM1P
,
LOC105374000
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271587
variant
18.

nsv3873905

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR5AC4P
,
LOC105373996
,
LOC105373999
,
OR5H15
,
OR5K3
,
POU5F1P7
,
LOC105374000
,
OR5K4
,
OR5H5P
,
RIOX2
,
OR5H7P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48437260
variant
19.

nsv6636342

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA6
,
OR5AC2
,
CRYBG3
,
OR5AC1
,
LOC101929298
,
GABRR3
,
ARL6
,
LOC105373994
,
OR5BM1P
,
RIOX2
Location information:
Clinical significance:
Uncertain significance
ID:
54355171
variant
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