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Items: 1 to 20 of 29

1.

nsv4675448

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-88P
,
LOC105376416
,
UPF2
,
DHTKD1
Location information:
Clinical significance:
Uncertain significance
ID:
50272273
variant
2.

nsv3914771

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COX6CP17
,
TUBAL3
,
LARP4B-DT
,
GAPDHP45
,
CDNF
,
LOC105376413
,
CDC123
,
RPP38-DT
,
IDI1
,
TASOR2
,
LINC00707
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478126
variant
3.

nsv3884983

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPA14
,
TASOR2
,
COX6CP17
,
GATA3-AS1
,
CDC123
,
CDNF
,
GAPDHP45
,
LOC105376413
,
ST8SIA6-AS1
,
RPP38-DT
,
RNA5SP302
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448338
variant
4.

nsv3911783

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928834
,
MEIG1
,
ATP5F1C
,
FAM171A1
,
NMT2
,
PPIAP30
,
LOC107984206
,
RBISP1
,
RSU1
,
NSUN6
,
ST8SIA6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475138
variant
5.

nsv3918372

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IL9RP2
,
PRKCQ
,
RNU6-1095P
,
LINC02656
,
AKR1C7P
,
BTBD7P1
,
LOC107984195
,
LOC107984198
,
LOC105379850
,
MIR3155B
,
PFKP-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481727
variant
6.

nsv3890577

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376364
,
LOC101930421
,
LOC105376344
,
LOC107984201
,
RNA5SP298
,
LOC105376384
,
ANKRD16
,
ECHDC3
,
LOC105376361
,
IDI2-AS1
,
LOC105376387
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453932
variant
7.

nsv3911206

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02656
,
NUDT5
,
RNU6-1095P
,
PROSER2-AS1
,
AKR1C7P
,
ASB13
,
PRKCQ
,
LOC105376395
,
CALML3-AS1
,
MIR3155B
,
LOC105376398
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474561
variant
9.

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
10.

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
11.

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
12.

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
13.

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
14.

nsv3904390

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00700
,
LINC02881
,
LINC01264
,
WDFY4
,
RNU6-908P
,
SNORD130
,
RPL36AP36
,
LOC107984175
,
BEND7-DT
,
COMMD3-BMI1
,
VSTM4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467745
variant
15.

nsv3920796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EPC1-AS1
,
RNU6-452P
,
AMD1P1
,
LYZL1
,
LOC105376415
,
RNU6-1075P
,
LOC107984192
,
LOC107984195
,
RN7SKP220
,
MACORIS
,
MIR4481
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484151
variant
16.

nsv6313952

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL36AP55
,
HNRNPA1P32
,
ABI1
,
MIR1915HG
,
LOC105376454
,
DNM1P17
,
RNA5SP305
,
LOC105376474
,
MINDY3
,
LOC107984205
,
RNU6-306P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677823
variant
17.

nsv3917667

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP241
,
DIP2C-AS1
,
RPL31P45
,
C10orf67-AS1
,
LOC107984207
,
LOC105376398
,
PROSER2
,
LOC107984210
,
RPL26P28
,
RPL6P24
,
RPL36AP36
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481022
variant
18.

nsv3924406

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
WDR37
,
LOC105376364
,
ST8SIA6-AS1
,
ANKRD16
,
RNA5SP300
,
FBH1
,
ECHDC3
,
LOC101930421
,
STAM-DT
,
LINC02654
,
LOC107984193
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487761
variant
19.

nsv3920285

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NRBF2P5
,
DDX20P1
,
DCLRE1CP1
,
LINP1
,
ITIH2
,
LOC105376409
,
NET1
,
SFTA1P
,
MEIG1
,
MSANTD7
,
CELF2-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483640
variant
20.

nsv4455607

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376357
,
LINC02649
,
LOC107984191
,
DIP2C
,
CELF2-AS1
,
LINC02669
,
LOC105376374
,
LOC107984168
,
LINC02668
,
RN7SL754P
,
RPL12P28
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621242
variant
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