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Items: 1 to 20 of 25

1.

nsv5380796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FAUP4
,
MMP7
,
SETP17
,
LUZP2
,
MIR6124
,
KCTD9P4
,
CCND1
,
RNU6-1238P
,
RNA5SP339
,
MMP10
,
GPR152
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51636053
variant
2.

nsv3904761

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS6P16
,
CTSC
,
LOC105369489
,
RN7SKP273
,
MTCYBP25
,
LOC105369469
,
CCDC81
,
LOC107984388
,
RNU6-560P
,
CASP4LP
,
LOC105369409
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468116
variant
3.

nsv3910101

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PHB1P16
,
LOC100418884
,
LOC101929174
,
SRSF8BP
,
C11orf54
,
SNORD13I
,
LINC02764
,
GRIA4
,
REXO2
,
PPIHP1
,
GPR83
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473456
variant
4.

nsv5672640

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPD1P13
,
CARD17P
,
SIK2
,
EXPH5
,
LOC100420803
,
WTAPP1
,
RN7SL222P
,
LOC112268081
,
CYCSP29
,
LOC107984381
,
SMARCE1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
52233775
variant
5.

nsv4455554

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02732
,
LINC02698
,
HOATZ
,
LOC105369489
,
C11orf71
,
LINC02703
,
RPS2P39
,
LOC107984385
,
LOC105369466
,
RPS12P21
,
LOC101928847
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621189
variant
6.

nsv4675680

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DRD2
,
NCAM1
,
LOC643855
,
CARD18
,
RNU7-187P
,
CASP1
,
GNG5P3
,
AASDHPPT
,
HNRNPA1P60
,
RAB39A
,
LOC105369474
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272505
variant
7.

nsv4675323

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPSAP50
,
RNA5SP349
,
NXPE1
,
NPAT
,
NNMT
,
DLAT
,
TEX12
,
FDXACB1
,
BCO2
,
LINC02719
,
ALG9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272148
variant
8.

nsv6637811

ID:
54356640
variant
9.

nsv4683939

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FDXACB1
,
LOC107984386
,
POU2AF1
,
RNU2-60P
,
PIH1D2
,
HOATZ
,
RN7SKP273
,
BTG4
,
CRYAB
,
CFAP68
,
PPIHP1
,
See more...
Location information:
Clinical significance:
Uncertain significance,
Pathogenic
ID:
50286619
variant
10.

nsv7093830

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100132078
,
DLAT
,
ALG9
,
DIXDC1
,
RNU6-893P
,
NKAPD1
,
MIR4491
,
CRYAB
,
LAYN
,
LOC644277
,
PPIHP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55274019
variant
11.

nsv7093915

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CRYAB
,
BTG4
,
LAYN
,
RN7SKP273
,
CFAP68
,
MIR4491
,
POU2AF3
,
PIH1D2
,
HOATZ
,
MIR34C
,
HSPB2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55274104
variant
12.

nsv7093916

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL37AP8
,
DIXDC1
,
RNU6-893P
,
FDXACB1
,
DLAT
,
ALG9
,
CRYAB
,
HSPB2
,
PPIHP1
,
CFAP68
,
PIH1D2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55274105
variant
13.

nsv3893233

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376598
,
OSBPL9P2
,
LOC100421985
,
NLRP10
,
GLB1L2
,
LINC02685
,
FTH1P16
,
PTS
,
SORL1-AS1
,
OR9G3P
,
OR8G5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456588
variant
14.

nsv3900144

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RTN3
,
KRTAP5-13P
,
LOC653503
,
LOC105376646
,
LOC105369539
,
MPPED2
,
DLG2
,
SORL1-AS1
,
YWHABP2
,
SCN3B
,
TRIM53AP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463499
variant
15.

nsv3908873

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHMBP2
,
SYTL2
,
LRRC32
,
RPS25
,
OR5AO1P
,
TREHP1
,
OR51A9P
,
CHRNA10
,
BATF2
,
GLYAT
,
PPP2R5B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472228
variant
16.

nsv6315537

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PYGM
,
ATL3
,
LOC105376656
,
LOC649133
,
RPL31P47
,
ALDH3B1
,
RNA5SP350
,
CATSPER1
,
MIR5582
,
MIR192
,
LOC105369571
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680484
variant
17.

nsv3898361

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SESN3
,
LOC107984352
,
AMOTL1
,
TRP-TGG2-1
,
LOC105369453
,
RPS3AP42
,
RN7SL786P
,
CASP12
,
ACER3
,
HIKESHI
,
LIPT2-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461716
variant
18.

nsv3922253

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS27P19
,
UBASH3B
,
USP2-AS1
,
USP28
,
PRR13P3
,
RN7SKP273
,
C11orf71
,
PRDM10-DT
,
SLN
,
LINC02698
,
SNORD14C
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485608
variant
19.

nsv6289927

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGSF9B
,
MIR10526
,
RPL37AP8
,
APOA5
,
PATE1
,
LOC105369579
,
LOC390255
,
TTC36
,
FDX1
,
LINC02719
,
TFAMP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53633439
variant
20.

nsv3913577

ID:
48476932
variant
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