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Items: 1 to 20 of 26

1.

nsv3919826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-438P
,
LOC105375300
,
URGCP
,
MOXD2P
,
LOC105375171
,
SP4
,
LOC105375194
,
LOC105375277
,
TRBV21-1
,
MIR4283-1
,
VN1R24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483181
variant
2.

nsv3888815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986817
,
DNAJB9
,
LRRN3
,
SKAP2
,
LOC107986794
,
MAGI2-AS2
,
CPA2
,
MIR10525
,
VN1R37P
,
SPDYE7P
,
DPY19L1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452170
variant
3.

nsv6313503

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GJC3
,
LAMB4
,
PVRIG2P
,
DUS4L-BCAP29
,
CBLL1-AS1
,
RN7SKP86
,
MIR4467
,
EIF4BP6
,
LOC107986835
,
CYP3A43
,
RELN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677374
variant
4.

nsv3903311

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLOD3
,
TRW-CCA5-1
,
SAP25
,
MIR106B
,
MCM7
,
LOC105375421
,
RPL7AP39
,
LOC100128334
,
CYP3AP2
,
TAF6
,
LINC01007
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466666
variant
9.

nsv3894780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-565P
,
LAMB1
,
MIR5707
,
LOC100419774
,
ZNF786
,
ELK1P1
,
MTCYBP42
,
SSU72L6
,
EEF1A1P27
,
LOC105375200
,
THUMPD3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458135
variant
10.

nsv4455091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP51
,
FLJ40288
,
STAG3L2
,
FKBP9
,
BNIP3P11
,
GPR37
,
LOC105375251
,
LOC100419642
,
LOC105375148
,
PMS2P7
,
TRBV10-3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49620726
variant
11.

nsv3909087

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MNX1-AS2
,
VN1R31P
,
PRSS58
,
LOC107986715
,
AHCYL2
,
BAIAP2L1
,
LOC107986821
,
NUPR2
,
SEPTIN7P4
,
PRKAR1B
,
TRBV15
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472442
variant
12.

nsv3908592

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRGV3
,
SNX10-AS1
,
LOC105375433
,
LOC101060796
,
OR9A2
,
LOC105375542
,
SPDYE2
,
NPY
,
RNU6-979P
,
RN7SL265P
,
RNY4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471947
variant
13.

nsv3922815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEPTIN7P6
,
MIR93
,
TAS2R4
,
RNA5SP247
,
RNU6-393P
,
LOC105375505
,
TRBV12-3
,
LOC107986829
,
CPSF4
,
GCC1
,
LOC349160
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486170
variant
14.

nsv3894097

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYP3A5
,
H2BK1
,
TRBC1
,
TRP-AGG2-3
,
CDC26P1
,
OR6B1
,
CPED1
,
LOC105375567
,
MTRNR2L6
,
ARHGEF35-AS1
,
PRSS2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457452
variant
15.

nsv5381780

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARPC1A
,
LOC112267858
,
STEAP4
,
GNB2
,
OR2AE1
,
SLC66A2P1
,
RN7SL478P
,
LOC100419447
,
LOC100131859
,
LOC101927610
,
CHCHD4P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51637037
variant
17.

nsv6315223

Variant type:
complex substitution
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AOC1
,
ACHE
,
ACTB
,
ADCY1
,
ADCYAP1R1
,
AEBP1
,
AHR
,
AKR1B1
,
AMPH
,
AOAH
,
AQP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680170
variant
18.

nsv4352523

Variant type:
inversion
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACHE
,
ADCY1
,
ADCYAP1R1
,
AEBP1
,
AMPH
,
AOAH
,
AQP1
,
ASL
,
ASNS
,
AZGP1
,
BLVRA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49347436
variant
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