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Items: 18

1.

nsv7137209

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-12P
,
RNU1-65P
,
AGAP6
,
RPL15P13
,
LHPP
,
MTCO2P23
,
CHAT
,
LINC02935
,
XRCC6P1
,
MIR548F1
,
ENTPD1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356054
variant
2.

nsv4675455

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRLN
,
LOC102724778
,
ANK3
,
AGAP14P
,
ANXA2P3
,
SLC16A9
,
LOC105378291
,
LOC105378311
,
FAM21EP
,
PARGP1-AGAP4
,
LOC105378314
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272280
variant
3.

nsv3922335

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UNC5B-AS1
,
ALDH7A1P4
,
LOC102724768
,
TET1
,
LOC107984235
,
ADK
,
VCL
,
RPS26P40
,
PHYHIPL
,
LOC105378350
,
MACROH2A2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485690
variant
5.

nsv3906389

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100419870
,
LOC102724439
,
LOC105378313
,
ELOVL3
,
MIR936
,
YWHAZP5
,
RN7SL394P
,
LOC105376398
,
PWWP2B
,
MIR4675
,
DUSP8P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469744
variant
6.

nsv3891157

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGAP14P
,
LOC100505502
,
LINC01514
,
LOC105378549
,
SIRT1
,
UROS
,
LOC105378443
,
KSR1P1
,
LOC105378314
,
LINC02663
,
LOC100130881
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454512
variant
7.

nsv3902271

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ANXA11
,
EDRF1-DT
,
TSPAN14
,
NUTM2A-AS1
,
LOC105378549
,
LINC02646
,
KCNMA1
,
RN7SKP196
,
LOC105376357
,
LOC105378552
,
GLRX3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465626
variant
8.

nsv3891958

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TUBB8
,
PPP2R2D
,
NRAP
,
LOC105376475
,
LOC101928834
,
LOC105376372
,
ITPRIP-AS1
,
LINC00702
,
LIPF
,
CASC2
,
RNU6-1090P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455313
variant
9.

nsv7137211

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EXOC6
,
VCL
,
EBAG9P1
,
LOC105378573
,
LINC01264
,
LINC02627
,
MED6P1
,
ALDH7A1P4
,
MIR4675
,
RPS27P18
,
SAMD8
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55356056
variant
10.

nsv3924859

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BMS1P4-AGAP5
,
MTCO2P23
,
DUSP13B
,
CCSER2
,
MIR4676
,
COMTD1
,
TMEM256P1
,
LINC00858
,
NUTM2B
,
TMEM14DP
,
VDAC2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48488214
variant
11.

nsv3917047

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC9A3P3
,
JMJD1C-AS2
,
LINC02637
,
SGMS1
,
LOC105378307
,
RPLP1P10
,
LOC105378327
,
RN7SL591P
,
LRRTM3
,
NODAL
,
MRPS35P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480402
variant
12.

nsv3921181

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGAP6
,
A1CF
,
ARHGAP22
,
GLUD1P2
,
DEPP1
,
NEFMP1
,
RNU6-543P
,
LOC105378287
,
SHLD2P1
,
RASGEF1A
,
HNRNPA3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484536
variant
14.

nsv3907664

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SHOC2
,
FAM245B
,
LINC00865
,
RN7SL840P
,
LOC107984179
,
DNMBP-AS1
,
RNY4P26
,
NT5C2
,
FAM149B1
,
RPS15AP5
,
PPP3CB-AS1
,
See more...
Location information:
Clinical significance:
drug response
ID:
48471019
variant
16.

nsv4674969

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-543P
,
ARID5B
,
JMJD1C-AS1
,
ALDH7A1P4
,
ZNF365
,
RN7SL591P
,
JMJD1C-AS2
,
LOC283045
,
LOC105378327
,
ADO
,
EGR2
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271794
variant
17.

nsv3921516

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF365
,
LOC283045
,
ARID5B
,
ALDH7A1P4
,
LOC105378323
,
LINC02625
,
RHOBTB1
,
CABCOCO1
,
RTKN2
,
LOC105378327
,
RN7SL591P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48484871
variant
18.

nsv3896400

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RTKN2
,
ADO
,
LINC02621
,
LOC107984012
,
EGR2
,
RN7SL591P
,
LOC105378327
,
LOC283045
,
ALDH7A1P4
,
ZNF365
Location information:
Clinical significance:
Uncertain significance
ID:
48459755
variant
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