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Items: 1 to 20 of 23

1.

nsv4455954

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BORCS7-ASMT
,
AS3MT
,
CNNM2
,
LOC107984265
Location information:
Clinical significance:
Uncertain significance
ID:
49621589
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.

nsv3920295

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EIF2S2P3
,
CYP17A1-AS1
,
MTND4P19
,
PRLHR
,
LBX1
,
ABRAXAS2
,
KLLN
,
WARS2P1
,
DUX4L28
,
PTPRE
,
LOC107984252
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483650
variant
4.

nsv3905499

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS15AP30
,
PDCD11
,
GBF1
,
MXI1
,
MARCKSL1P1
,
LOC101927573
,
RNU11-3P
,
PFN1P11
,
SHOC2
,
INA
,
ATP5MK
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468854
variant
5.

nsv3916477

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
XPNPEP1
,
NRAP
,
HMGB3P5
,
GSTO1
,
MIR1307
,
LOC107984266
,
ITPRIP
,
COL17A1
,
RNA5SP325
,
LOC105378464
,
RN7SKP288
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479832
variant
6.

nsv3924696

ID:
48488051
variant
7.

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
8.

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
9.

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
10.

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
11.

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
12.

nsv3905489

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378476
,
SMC3
,
EIF2S2P3
,
PDZD8
,
PRDX3
,
TBC1D12
,
FGF8
,
HSPA12A-AS1
,
LINC00601
,
CYP17A1-AS1
,
SPCS2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468844
variant
13.

nsv3890046

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UROS
,
KCNK18
,
LOC105378549
,
C10orf88B
,
LINC02646
,
MIR548E
,
GLRX3
,
EEF1AKMT2
,
SUFU
,
CHST15
,
RN7SL749P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453401
variant
14.

nsv3921919

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4295
,
BORCS7
,
RN7SL524P
,
GPAM
,
STN1
,
ZRANB1
,
LOC105378521
,
PSD
,
MIR1307
,
CTBP2
,
DENND10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485274
variant
15.

nsv3898332

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NPS
,
BTF3P15
,
CPXM2
,
RN7SL749P
,
UROS
,
OR6L2P
,
DUX4L13
,
RPL19P16
,
NFKB2
,
LOC107984128
,
LOC724065
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461687
variant
16.

nsv3923769

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378493
,
LINC02627
,
RPL23AP59
,
ADAM12
,
PPIAP39
,
LOC105378490
,
FBXL15
,
C10orf95-AS1
,
PTGES3P4
,
CCDC172
,
PCGF6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487124
variant
17.

nsv3909942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102723665
,
SFR1
,
RNU6-839P
,
PNLIP
,
DNTT
,
MIR4685
,
ARL3
,
MIR3158-1
,
RPL7P35
,
LOC105378492
,
LOC107984265
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473297
variant
18.

nsv3900811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARL3
,
CYP17A1
,
NFKB2
,
PITX3
,
PSD
,
TAF5
,
GBF1
,
INA
,
NEURL1
,
NOLC1
,
ACTR1A
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48464166
variant
19.

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
20.

nsv3894450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HPS1
,
LOC112268063
,
RRP12
,
MED6P1
,
WNT8B
,
LOC105378447
,
LOC105378424
,
LOC105378401
,
LOC107984263
,
ARL3
,
TLL2
,
See more...
Location information:
Clinical significance:
drug response
ID:
48457805
variant
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