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Items: 1 to 20 of 48

4.

nsv7094682

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP428
,
PHAF1
,
CA7
,
CES3
,
FBXL8
,
CES2
,
LOC105371316
,
DYNC1LI2-DT
,
CMTM3
,
MATCAP1
,
RRAD
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55274871
variant
5.

nsv3918405

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLEKHG4
,
TMEM208
,
TPPP3
,
CDH5
,
LOC105371318
,
DYNC1LI2-DT
,
RN7SL543P
,
SLC9A5
,
FHOD1
,
RN7SKP118
,
KCTD19
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481760
variant
6.

nsv3923505

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DYNC1LI2
,
CIAO2B
,
LRRC36
,
LOC107984881
,
MIR328
,
EXOC3L1
,
FBXL9P
,
LOC107984821
,
HSD11B2
,
NUTF2
,
PDP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486860
variant
7.

nsv4350223

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CBFB
,
B3GNT9
,
KARS1P3
,
CARMIL2
,
NFATC3
,
RNU1-123P
,
CENPT
,
AGRP
,
PARD6A
,
DPEP2
,
CTRL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49345136
variant
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

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
17.

nsv3913913

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATP5F1AP3
,
LOC105371414
,
HSDL1
,
CPHXL2
,
LOC100131126
,
ZC3H18-AS1
,
LOC101928474
,
NUDT7
,
LOC107984816
,
SPATA33
,
CBFB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477268
variant
18.

nsv3919817

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376772
,
WWP2
,
RNU6-208P
,
LOC101928682
,
HSPE1P5
,
CMTM2
,
LINC02136
,
LOC112268169
,
FANCA
,
LOC105371376
,
TAT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483172
variant
19.

nsv3910304

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MC1R
,
LOC107984856
,
MIR3182
,
NAE1
,
PARD6A
,
LINC00922
,
TCF25
,
ATP2C2-AS1
,
PLEKHG4
,
LOC100418868
,
LINC01082
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473659
variant
20.

nsv3920399

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC654780
,
LSM3P5
,
DHODH
,
ZNF23
,
EXOSC6
,
LOC105371311
,
LOC105371308
,
MTCYBP28
,
PKD1L3
,
LOC105371328
,
RNA5SP433
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483754
variant
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