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Items: 1 to 20 of 41

1.

nsv3906951

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF319
,
USB1
Location information:
Clinical significance:
Benign
ID:
48470306
variant
2.

nsv3891356

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMP15
,
USB1
Location information:
Clinical significance:
Likely benign
ID:
48454711
variant
3.

nsv3906560

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
USB1
,
ZNF319
Location information:
Clinical significance:
Benign
ID:
48469915
variant
4.

nsv3891054

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMP15
,
ZNF319
,
USB1
Location information:
Clinical significance:
Benign
ID:
48454409
variant
5.

nsv3916542

ID:
48479897
variant
9.

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
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

nsv3915506

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CFAP69P1
,
GAS8-AS1
,
LOC105371354
,
RNU6-22P
,
MIR6775
,
TERB1
,
RN7SL841P
,
CFDP1
,
JPH3
,
LOC105371351
,
RNU6-1153P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478861
variant
17.

nsv3891306

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984894
,
BEAN1
,
MPHOSPH6
,
LOC100419639
,
SNAI3
,
KLHL36
,
RNU1-103P
,
SNORA50A
,
LOC107984897
,
LOC105371335
,
LINC02132
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454661
variant
18.

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
19.

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
20.

nsv3893486

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF19
,
CKLF-CMTM1
,
RNU4-30P
,
AARS1
,
LOC105371298
,
LOC105371301
,
APOOP5
,
CSNK2A2
,
CDH11
,
CCDC113
,
NUP93
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456841
variant
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