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Items: 1 to 20 of 78

1.

nsv3919826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-438P
,
LOC105375300
,
URGCP
,
MOXD2P
,
LOC105375171
,
SP4
,
LOC105375194
,
LOC105375277
,
TRBV21-1
,
MIR4283-1
,
VN1R24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483181
variant
2.

nsv4675615

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATG9B
,
OR10AC1
,
LOC100420648
,
INSIG1
,
TRC-GCA9-3
,
RNU6-1184P
,
OR6V1
,
OR2A5
,
LUZP6
,
BLACE
,
AGBL3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272440
variant
3.

nsv3915633

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MOXD2P
,
CALD1
,
LOC101927914
,
TRBV6-1
,
MGAM2
,
REPIN1-AS1
,
TRC-GCA17-1
,
ZNF783
,
GIMAP7
,
RNF32-DT
,
TRBV5-6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478988
variant
4.

nsv3897512

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375548
,
RNA5SP250
,
TRBV5-7
,
WBP1LP1
,
TRBV22-1
,
LOC105375571
,
ZC3HAV1
,
INSIG1-DT
,
AGK
,
LOC105375588
,
UBE3C
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48460867
variant
5.

nsv3903590

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375597
,
LOC101928466
,
TRC-GCA11-1
,
TAS2R39
,
PRKAG2
,
ATP6V0E2
,
TRC-GCA19-1
,
LOC105375557
,
TRC-GCA3-1
,
ETF1P2
,
LOC105375537
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466945
variant
6.

nsv3910344

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268012
,
EPHA1-AS1
,
BRAF
,
CNTNAP2-AS1
,
WEE2-AS1
,
TRBV6-5
,
PRKAG2-AS1
,
RPL36AP28
,
VIPR2
,
LOC105375556
,
LOC105375536
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473699
variant
7.

nsv3905379

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AGAP3
,
OR2A7
,
LOC105375584
,
TRC-GCA9-3
,
TRC-GCA1-1
,
OR6B1
,
ZNF775-AS1
,
ATG9B
,
KMT2C
,
BLACE
,
INSIG1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468734
variant
8.

nsv3919772

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375567
,
LOC389602
,
FABP5P3
,
ZNF775-AS1
,
TRBV1
,
LOC154761
,
TRC-GCA1-1
,
LOC402715
,
OR2A1
,
KMT2C
,
GIMAP3P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483127
variant
9.

nsv3904188

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RBM33-DT
,
OR2A20P
,
TRBV16
,
LOC102723795
,
INSIG1-DT
,
PAICSP6
,
CTAGE8
,
ATP6V0E2-AS1
,
LOC100134040
,
TRC-GCA13-1
,
CRYGN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467543
variant
10.

nsv3915683

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FASTK
,
LOC107986721
,
LOC105375566
,
THAP5P1
,
TRC-GCA16-1
,
ZNF212
,
NCAPG2
,
CNTNAP2
,
PAXIP1-AS2
,
DNAJB6
,
LOC105375592
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479038
variant
11.

nsv3907788

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GIMAP1
,
MNX1-AS2
,
MIR5707
,
OR2AO1P
,
LOC643438
,
OR2A1-AS1
,
TRC-GCA21-1
,
TRC-GCA17-1
,
ZNF767P
,
TRC-GCA20-1
,
REPIN1-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471143
variant
12.

nsv3918396

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL845P
,
LINC01003
,
ATP5PBP3
,
ATP6V0E2-AS1
,
PRKAG2
,
ETF1P2
,
ABCF2-H2BK1
,
LOC645272
,
DPP6
,
LOC100134040
,
LOC105375594
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481751
variant
13.

nsv3924350

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986750
,
LOC107986856
,
MIR671
,
RPL36AP30
,
LINC00244
,
LOC105375578
,
GIMAP3P
,
TRC-GCA9-2
,
TMEM176A
,
XRCC2
,
FABP5P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487705
variant
14.

nsv4675268

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ABCB8
,
THAP5P1
,
DNAJB6
,
LOC107986856
,
FASTK
,
LOC777650
,
XRCC2
,
EIF2AP3
,
ZNF746
,
LOC105375601
,
RN7SL76P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272093
variant
15.

nsv3923268

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AOC1
,
LOC105375602
,
RNU7-20P
,
LOC100301516
,
RNU6-604P
,
LOC105375579
,
LOC105375599
,
GIMAP5
,
MIR595
,
NOM1
,
LOC105375559
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486623
variant
16.

nsv3923788

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375582
,
RPL36AP28
,
LOC102723686
,
LOC105375602
,
LOC105375559
,
TRC-GCA10-1
,
LOC105375579
,
LOC112268012
,
LOC105375599
,
C7orf33
,
LINC03010
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487143
variant
17.

nsv3920858

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP250
,
RN7SL845P
,
RHEB
,
RNU4-31P
,
MNX1-AS1
,
LOC105375571
,
ZBED10P
,
DPP6
,
UBE3C
,
TRPC6P3
,
ZNF775
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484213
variant
18.

nsv3914838

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
WDR86-AS1
,
GIMAP8
,
PAXIP1-DT
,
LOC777650
,
LMBR1
,
ALDH7A1P3
,
LOC101928733
,
DUTP3
,
LINC00244
,
ZNF746
,
TRC-GCA22-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478193
variant
19.

nsv3900730

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EZH2
,
LOC105375578
,
TRC-GCA9-2
,
LOC105375581
,
RN7SL76P
,
EN2
,
TRC-GCA15-1
,
CHPF2
,
ABCB8
,
TRC-GCA12-1
,
LOC105375604
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464085
variant
20.

nsv6290897

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRC-GCA21-1
,
LINC00996
,
GIMAP1
,
GALNTL5
,
TRC-GCA20-1
,
RNF32
,
LOC105375589
,
MIR5707
,
MNX1-AS2
,
LOC285889
,
GIMAP7
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53636292
variant
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