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Items: 20

1.

nsv6309157

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SIRT1
Location information:
Clinical significance:
Uncertain significance
ID:
53673028
variant
2.

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
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
4.

nsv3917822

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MYL6P3
,
CHCHD1
,
AKR1B10P1
,
LOC107984239
,
LINC02671
,
RN7SL840P
,
RPS3AP37
,
FAM149B1
,
ANXA2P3
,
LOC101929846
,
PLA2G12B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481177
variant
5.

nsv6314185

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC25A16
,
CTNNA3
,
ATOH7
,
MYPN
,
ASCC1
,
COX20P1
,
RPS26P42
,
ADAMTS14
,
MIR7151
,
LINC02636
,
MCU
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53678056
variant
6.

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
7.

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
8.

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
9.

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
10.

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
11.

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
12.

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
13.

nsv3891070

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NRG3-AS1
,
FAM32CP
,
ZNF503-AS1
,
LOC105378358
,
TNPO1P1
,
MTND1P20
,
RPL11P3
,
RPS26P40
,
PTEN
,
LINC00502
,
RN7SL220P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48454425
variant
14.

nsv3917966

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02640
,
HK1
,
VDAC2
,
EIF4A2P2
,
MTCO2P23
,
DLG5-AS1
,
COMTD1
,
TMEM256P1
,
MIR4676
,
RPS24
,
HKDC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481321
variant
15.

nsv3899672

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DNA2
,
HNRNPH3
,
SLC25A16
,
SIRT1
,
HERC4
,
CTNNA3
,
RUFY2
,
CCAR1
,
DNAJC12
,
PBLD
,
DDX50
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48463027
variant
16.

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
18.

nsv4675581

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL220P
,
TRS-TGA1-1
,
RN7SKP202
,
POU5F1P5
,
RN7SL394P
,
LINC02640
,
RPL21P92
,
DNAJC12
,
RNU6-1250P
,
SIRT1
,
MIR7151
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50272406
variant
19.

nsv4675035

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
POU5F1P5
,
RN7SL394P
,
RPL12P8
,
RNU6-1250P
,
RPS3AP38
,
MYPN
,
HERC4
,
RNU6-523P
,
RPL21P92
,
RN7SL220P
,
SIRT1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50271860
variant
20.

nsv6637501

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL220P
,
HERC4
,
RN7SL394P
,
RPS3AP38
,
MYPN
,
LOC107984240
,
RNU6-523P
,
DNAJC12
,
SIRT1
,
DNAJC19P1
,
POU5F1P5
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
54356330
variant
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