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Items: 1 to 20 of 53

1.

nsv4457441

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FDX1P2
,
GABPA
,
ATP5PF
,
JAM2
Location information:
Clinical significance:
Uncertain significance
ID:
49623076
variant
2.

nsv4457572

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATP5PF
,
JAM2
,
FDX1P2
,
GABPA
Location information:
Clinical significance:
Uncertain significance
ID:
49623207
variant
3.

nsv3908183

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
JAM2
,
GABPA
,
LLPHP2
,
ATP5PF
Location information:
Clinical significance:
Uncertain significance
ID:
48471538
variant
4.

nsv3923176

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COL18A1-AS2
,
RCAN1
,
C21orf91-OT1
,
KRTAP13-2
,
KRTAP19-9P
,
VN2R20P
,
CYCSP42
,
HSPA13
,
RNU6-772P
,
BACH1-IT2
,
KRTAP25-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486531
variant
5.

nsv3905423

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND5P1
,
RPL37P3
,
PRDM15
,
PLAC4
,
C21orf62-AS1
,
MIR6814
,
DYRK1A
,
ITSN1
,
LINC00649
,
SETD4
,
LRRC3-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468778
variant
6.

nsv3917693

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DPRXP5
,
MIR6724-1
,
ZNF299P
,
KRTAP22-1
,
TMPRSS15
,
CHODL-AS1
,
MIR4759
,
LOC105369299
,
LOC105372774
,
OLIG1
,
MTRES1P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481048
variant
7.

nsv3922838

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL163P
,
LOC105372759
,
RNU1-139P
,
TPTE
,
SNX18P13
,
LOC107985511
,
PPIAP1
,
LOC105372762
,
C21orf91
,
VN1R109P
,
CYP2C63P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486193
variant
8.

nsv3916181

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADAMTS5
,
LINC00307
,
RNU6-772P
,
KRTAP25-1
,
HSPD1P7
,
KRT18P2
,
LINC01683
,
ATP5PF
,
HSPA13
,
KRTAP19-9P
,
LINC01673
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479536
variant
9.

nsv3920431

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF114P1
,
MIR3118-1
,
RPL13AP7
,
RPL37P3
,
MARCKSP1
,
LOC105372749
,
GXYLT1P2
,
ADAMTS1
,
HSPD1P7
,
LINC02573
,
ANKRD20A11P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483786
variant
10.

nsv4676306

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
JAM2
,
LINC01549
,
LOC105372762
,
LOC105372745
,
MIR99A
,
RN7SKP236
,
LOC107985494
,
USP25
,
RNU6-1326P
,
FRG2MP
,
LOC107985474
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50273131
variant
11.

nsv3921072

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYYR1-AS1
,
RNU1-98P
,
BTG3
,
ADAMTS1
,
MARCKSP1
,
LINC01684
,
KRT18P2
,
LOC107985483
,
ASMER1
,
RPL37P3
,
MSANTD2P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484427
variant
12.

nsv3909006

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372738
,
MIR8069
,
LOC654338
,
LOC105372758
,
SLC6A6P1
,
RNU2-55P
,
BTF3L4P1
,
LOC101927745
,
TUBAP1
,
RNA5SP488
,
GPX1P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472361
variant
13.

nsv3917277

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SREK1IP1P1
,
LINC00308
,
LOC105369304
,
RN7SL163P
,
LOC105372759
,
RNU1-139P
,
LOC105372762
,
CYP2C63P
,
JAM2
,
RNU6-1326P
,
C21orf91
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480632
variant
14.

nsv3915265

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TUBAP1
,
LOC105372775
,
RNU2-55P
,
N6AMT1
,
FBXW11P1
,
MIR4327
,
KRTAP22-2
,
RN7SKP147
,
LINC00161
,
KRTAP13-4
,
LOC105372758
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478620
variant
15.

nsv3923006

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KRTAP23-1
,
LOC105372750
,
SOD1-DT
,
HMGN1P2
,
LOC107985516
,
LOC105372770
,
LINC00515
,
LOC105372747
,
RPL23P2
,
LINC01687
,
CLDN17
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486361
variant
16.

nsv7096278

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
APP
,
GABPA
,
LOC105372756
,
LOC105372757
,
RNU6-123P
,
LLPHP2
Location information:
Clinical significance:
Pathogenic
ID:
55276467
variant
17.

nsv3914461

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00945
,
MIR6508
,
FRGCA
,
UMODL1-AS1
,
KRTAP8-3P
,
RPL23AP4
,
DSCR9
,
GET1
,
LINC00317
,
MTCYBP21
,
CHODL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477816
variant
18.

nsv3916732

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR6724-4
,
LOC105369306
,
TSPEAR-AS1
,
DOP1B
,
SIK1
,
EVA1C
,
MIR8069
,
RNA5SP491
,
LINC02943
,
RNA5SP488
,
DIP2A-IT1
,
See more...
Location information:
Clinical significance:
Uncertain significance,
Pathogenic
ID:
48480087
variant
19.

nsv3917878

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
POLR2CP1
,
LOC105372774
,
SNORA80A
,
PIGP
,
PSMD4P1
,
KRTAP21-3
,
RBMX2P1
,
CYYR1-AS1
,
IL10RB-DT
,
LOC105372797
,
POFUT2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481233
variant
20.

nsv3921828

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
U2AF1
,
S100B
,
LOC107985513
,
LOC107987299
,
ZBTB21
,
MIR155HG
,
LOC105372738
,
LINC01700
,
CDC27P10
,
MIR8069
,
KRTAP11-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485183
variant
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