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Items: 1 to 20 of 23

1.

nsv7096921

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IAH1
,
ADAM17
Location information:
Clinical significance:
Pathogenic
ID:
55277110
variant
2.

nsv4683899

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADAM17
,
IAH1
Location information:
Clinical significance:
Uncertain significance
ID:
50286579
variant
3.

nsv4681081

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADAM17
,
IAH1
Location information:
Clinical significance:
Uncertain significance
ID:
50283761
variant
4.

nsv3908896

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-1288P
,
MIR7515HG
,
ID2-AS1
,
LOC100506405
,
LOC105373424
,
RNA5SP84
,
RN7SL832P
,
LOC105373404
,
LOC100130731
,
LOC105373421
,
MIR4429
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48472251
variant
5.

nsv7096918

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITGB1BP1
,
LINC00299
,
MBOAT2
,
LOC101929643
,
LOC105373419
,
LOC105373422
,
ID2
,
LINC00298
,
ID2-AS1
,
KLF11
,
SNRPEP5
,
See more...
Location information:
Clinical significance:
Uncertain significance,
Pathogenic
ID:
55277107
variant
6.

nsv6315390

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268439
,
RNA5SP116
,
FAP
,
EIF3EP3
,
LOC107985821
,
LOC105373602
,
SLC44A3P1
,
LOC100420775
,
LOC100506405
,
RGPD6
,
FAR2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680337
variant
7.

nsv3874648

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGKV2OR2-10
,
LOC105374848
,
RN7SL313P
,
MIR3131
,
LOC107985957
,
RN7SKP179
,
EPCAM
,
RNU6-282P
,
LOC102723825
,
BOK
,
CD8B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438003
variant
8.

nsv3885544

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-674P
,
KANSL3
,
KHK
,
TM4SF20
,
ABCB11
,
BAZ2B-AS1
,
LOC105373506
,
ELOCP21
,
LOC105373612
,
LOC107985854
,
LOC107985960
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448899
variant
9.

nsv3882615

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND2P22
,
LOC112268410
,
ASIC4
,
LOC107985792
,
HAAO
,
RPL28P2
,
TRE-CTC7-1
,
RNU6-915P
,
CCDC138
,
LOC107986001
,
IGKV3D-7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445970
variant
10.

nsv3908605

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC35F6
,
LOC105374458
,
RPL21P70
,
CDPF1P1
,
RHOB
,
RN7SKP119
,
RPS27AP7
,
LOC107985808
,
LOC105373399
,
LOC105374590
,
CTBP2P5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471960
variant
11.

nsv3908288

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ALLC
,
LOC105373429
,
LINC01830
,
SLC66A3
,
MYCNUT
,
NDUFAF2P1
,
LINC01318
,
LINC01460
,
LOC105373346
,
LOC105374325
,
TAF1B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471643
variant
12.

nsv6636815

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374455
,
RN7SL674P
,
E2F6
,
NBAS
,
RPL21P70
,
LOC105374458
,
MAPRE3-AS1
,
RNU6-961P
,
DDX50P1
,
DDX1
,
MYCN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355644
variant
13.

nsv3908038

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373394
,
PGAM1P6
,
TMEM214
,
LINC01874
,
ASAP2
,
SLC7A15P
,
LOC105374453
,
LINC01875
,
GTF3C2
,
YWHAQ
,
RN7SKP112
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471393
variant
14.

nsv3907033

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GTF3C2-AS1
,
LOC105373399
,
E2F6
,
LOC105374378
,
OST4
,
ITSN2
,
LINC01804
,
MAPRE3-AS1
,
RNU6-649P
,
RN7SL674P
,
LOC100422227
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470388
variant
15.

nsv3893260

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC102723389
,
LOC105373433
,
MIR548S
,
LOC105374329
,
LOC105373436
,
GAPDHP48
,
LOC107985842
,
LOC107985839
,
MYT1L-AS1
,
ODC1
,
MBOAT2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456615
variant
16.

nsv3896997

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373359
,
MYT1L-AS1
,
LOC101929551
,
DDX1
,
EIPR1
,
RN7SL117P
,
MIR3681
,
LOC107985807
,
KCNF1
,
SH3YL1
,
RRM2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48460352
variant
17.

nsv3908459

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EIF1P7
,
LOC105373398
,
PIK3CDP1
,
TMSB4XP2
,
LOC107985855
,
LOC105373401
,
LOC105373395
,
RNFT1P1
,
KLF11-DT
,
KCNS3
,
LINC01247
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471814
variant
18.

nsv3908405

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100996549
,
LOC105373479
,
LINC00298
,
ADAM17
,
LOC101929551
,
RPL30P3
,
ODC1
,
MYT1L-AS1
,
ZPAXP
,
NACAP9
,
RNU7-176P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471760
variant
19.

nsv3886834

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01249
,
ID2-AS1
,
LOC100506405
,
TRIB2
,
LOC107985841
,
RNF144A
,
LOC105373438
,
LOC105373415
,
LINC00487
,
LOC105373395
,
ID2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48450189
variant
20.

nsv3908628

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS7
,
RPL30P3
,
FLJ33534
,
LOC101929691
,
ACP1
,
LOC105373398
,
RRM2
,
LOC105373421
,
LOC100130731
,
MIR4429
,
GREB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471983
variant
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