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Items: 1 to 20 of 31

1.

nsv3899037

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TOX3
,
LINC03064
,
LOC105371265
,
CASC16
Location information:
Clinical significance:
Uncertain significance
ID:
48462392
variant
5.

nsv3906108

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CKLF
,
NPIPP1
,
LOC100421169
,
MT1F
,
RNU6-1061P
,
PRM3
,
MYL11
,
GNG13
,
LOC105371316
,
IGHV3OR16-16
,
NFAT5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469463
variant
6.

nsv3904593

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100128079
,
LOC105379474
,
PKD1P4
,
DDX19A-DT
,
C16orf95-DT
,
LOC105371259
,
MIR6126
,
LOC105371050
,
TRP-CGG1-2
,
HBA1
,
SLC7A6OS
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467948
variant
7.

nsv3901410

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02175
,
FCSK
,
SNX29
,
HBQ1
,
TCF25
,
SNORD13H
,
LOC105371291
,
RNU6-159P
,
MIR548H2
,
LOC652276
,
TRAF7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464765
variant
8.

nsv3909417

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRSS53
,
LINC02134
,
DUX4L47
,
ZDHHC1
,
ZDHHC7
,
RPS26P51
,
LOC105371344
,
LCMT1-AS1
,
RPL7L1P19
,
RN7SL143P
,
LOC729217
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472772
variant
9.

nsv3892266

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FTLP14
,
ZNF785
,
TP53TG3
,
PDXDC1
,
PDZD9
,
PRR35
,
CAPNS2
,
MIR3179-2
,
ATP2A1-AS1
,
CFAP20
,
PRSS30P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455621
variant
10.

nsv3921269

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105371237
,
IGHV3OR16-11
,
SPMIP8
,
GAN
,
LOC105371343
,
CES5A
,
LSM3P5
,
LOC107984819
,
RNU6-103P
,
MIR138-2
,
CTRB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484624
variant
11.

nsv6314755

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATMIN
,
ATP6V0D1
,
CMPK1P2
,
HP
,
CENPBD1P
,
LOC105371399
,
COTL1
,
LOC105371293
,
TANGO6
,
LOC102723373
,
LOC107984827
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53678778
variant
12.

nsv3895555

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RSPRY1
,
LOC102723560
,
LOC105371268
,
CLUHP11
,
LOC105371265
,
CES1P1
,
GNAO1-AS1
,
RNU4-58P
,
ADGRG3
,
UBE2MP1
,
MIR6863
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458910
variant
13.

nsv3918521

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYLD-AS2
,
MT1F
,
ATP6V0D1
,
EDC4
,
LINC02178
,
LOC105371271
,
RNU6-1153P
,
LOC100421258
,
MT1L
,
TRL-CAG2-1
,
CTCF-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481876
variant
14.

nsv6637586

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02140
,
LOC100130602
,
CKBP1
,
FTO-IT1
,
NPAP1L
,
RN7SL841P
,
RNU6-20P
,
LOC112268167
,
CFAP69P1
,
LOC105371243
,
RPL31P56
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356415
variant
15.

nsv6112700

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CPNE2
,
USB1
,
RPL12P36
,
NDRG4
,
MOCS1P1
,
LOC101929000
,
RNU6-257P
,
C16orf78
,
LOC107984867
,
LOC102724859
,
CFAP20
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150545
variant
16.

nsv3912769

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MAF
,
LOC112268167
,
CHMP1A
,
VAC14-AS1
,
LOC101928502
,
LOC100421258
,
URAHP
,
WFDC1
,
TMEM231
,
MIR7854
,
RNA5SP418
,
See more...
Location information:
Clinical significance:
Benign
ID:
48476124
variant
17.

nsv3915341

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GINS3
,
LINC00919
,
LOC105371318
,
CHTF8
,
SALL1
,
RNA5SP428
,
ACTR3BP3
,
C16orf86
,
DUX4L45
,
UTP4
,
DRC7
,
See more...
Location information:
Clinical significance:
Benign
ID:
48478696
variant
18.

nsv3915118

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZFHX3
,
CENPN-AS1
,
RPS27AP16
,
LOC105371381
,
LOC100422275
,
TRM-CAT6-1
,
RN7SL520P
,
KLHL36
,
TAT-AS1
,
MIR4722
,
LOC388282
,
See more...
Location information:
Clinical significance:
Benign
ID:
48478473
variant
19.

nsv3912663

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SMG1P7
,
LOC105371287
,
LINC03064
,
LOC100420066
,
PPIAP49
,
BCAP31P1
,
SLC12A4
,
MIR9901
,
PLLP
,
RN7SKP118
,
PDXDC2P
,
See more...
Location information:
Clinical significance:
Benign
ID:
48476018
variant
20.

nsv3912156

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IST1
,
CMTR2
,
RN7SL841P
,
AFG3L1P
,
LOC107984901
,
EXOSC6
,
LINC02179
,
RNU6-1061P
,
CARMIL2
,
HSBP1
,
CLUHP11
,
See more...
Location information:
Clinical significance:
Benign
ID:
48475511
variant
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