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Items: 1 to 20 of 21

1.

nsv3883359

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
Benign
ID:
48446714
variant
2.

nsv3879218

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
Benign
ID:
48442573
variant
3.

nsv3887669

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
Benign
ID:
48451024
variant
4.

nsv3884448

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
not provided
ID:
48447803
variant
5.

nsv3888652

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
Uncertain significance
ID:
48452007
variant
6.

esv3648993

Variant type:
copy number variation
Associated study:
estd216
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
not provided
ID:
24503389
variant
7.

esv3648117

Variant type:
copy number variation
Associated study:
estd216
Organism:
human
Genes(s) in region:
EPHA3
Location information:
Clinical significance:
not provided
ID:
24503227
variant
8.

nsv3876149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTATP6P6
,
MTCO2P6
,
MTCO1P6
,
MTCO3P6
,
EPHA3
Location information:
Clinical significance:
Benign
ID:
48439504
variant
9.

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
13.

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
14.

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
15.

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
17.

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
18.

nsv3874413

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPE1P19
,
MTCO3P6
,
EPHA3
,
PROS2P
,
MTATP6P6
,
RNU6-712P
,
MTCO1P6
,
MTCO2P6
Location information:
Clinical significance:
Benign
ID:
48437768
variant
19.

nsv6291230

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-712P
,
NDUFA5P5
,
LOC105377202
,
MTCO1P6
,
MTCO2P6
,
ICE2P2
,
EPHA3
,
MTCO3P6
,
GAPDHP50
,
PROS2P
,
CGGBP1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53636625
variant
20.

nsv4674450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTCO2P6
,
PROS2P
,
EPHA3
,
MTCO3P6
,
HSPE1P19
,
MTATP6P6
,
RNU6-712P
,
MTCO1P6
Location information:
Clinical significance:
Uncertain significance
ID:
50271275
variant
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