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Items: 20

1.

nsv3881313

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IL19
,
LOC107985250
,
RPL13AP11
,
LOC105372873
,
SYT14
,
LPGAT1
,
RNASEH1P3
,
ATP5MC2P1
,
LINC01717
,
NUAK2
,
LOC105372887
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48444668
variant
2.

nsv3877365

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARK1
,
LINC02766
,
FDPS
,
PRUNE1
,
GJB4
,
RN7SL653P
,
PPIEL
,
CRB1
,
SELENBP1
,
LBR
,
CHML
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440720
variant
3.

nsv3885206

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP47
,
STK40
,
RNU6-750P
,
LINC01138
,
MIR4632
,
LOC107985100
,
EIF2D
,
SEPTIN7P13
,
RAB13
,
LOC107985524
,
DR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448561
variant
4.

nsv3884414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU1-153P
,
MIR3917
,
LOC105378793
,
CCDC190
,
RPL29P6
,
RUNX3-AS1
,
MIXL1
,
LCE1B
,
NAXE
,
PDC-AS1
,
BNIPL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447769
variant
5.

nsv4450583

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RGS18
,
LINC02257
,
RNA5SP79
,
ZP4
,
C1orf35
,
LOC101060016
,
LOC100271717
,
LOC100130137
,
LINC00303
,
LOC100420255
,
MIR1537
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49616218
variant
6.

nsv3881012

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372928
,
OR2T27
,
LOC107985251
,
RNA5S12
,
IRF6
,
LOC105373163
,
TRK-TTT3-2
,
GPATCH2
,
HHIPL2
,
LOC105371694
,
VASH2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48444367
variant
7.

nsv6634372

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373279
,
YBX1P9
,
RPL34P6
,
OR14C36
,
MIPEPP2
,
DSTYK
,
LINC01737
,
CDCA4P3
,
VN1R5
,
TMEM9
,
RNU6-1089P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54348675
variant
8.

nsv4674140

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5S8
,
NTPCR
,
ZNF496-DT
,
OR2L8
,
PTPN14
,
RPL13AP11
,
LEFTY3P
,
LINC01132
,
OR2L13
,
ACBD3-AS1
,
MIR215
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50270965
variant
9.

nsv3895767

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985458
,
SLC45A3
,
LOC107985243
,
LOC105371687
,
IGFN1
,
CDCA4P4
,
CSRP1-AS1
,
LAMB3
,
LOC105371664
,
LOC105372898
,
C1orf53
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459122
variant
10.

nsv3889347

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR1231
,
PTPN14
,
TUBA5P
,
LINC00538
,
LOC100131939
,
RNA5SP75
,
SEPTIN14P12
,
MYOG
,
LINC01698
,
UCHL5
,
SLC26A9-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452702
variant
11.

nsv6636965

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRELP
,
SYT14
,
SLC30A1
,
SNORA16B
,
PM20D1-AS1
,
PEBP1P3
,
RN7SKP156
,
PPP1R15B
,
HMGN1P4
,
LOC100421343
,
ARPC5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355794
variant
12.

nsv3879807

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RABIF
,
CFAP144P3
,
GARIN4
,
LINC00210
,
UBE2T
,
LOC101929305
,
LOC105371693
,
ANGEL2
,
LOC105372924
,
LOC105372901
,
BMNCR
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443162
variant
13.

nsv3892738

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HLX
,
SNORA16B
,
LOC105372984
,
LOC105372878
,
LPGAT1-AS1
,
NVL
,
PM20D1-AS1
,
NXNP1
,
XRCC6P3
,
SYT14
,
USH2A-AS2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456093
variant
15.

nsv3870877

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL13AP8
,
YOD1
,
PFKFB2
,
IL20
,
TRP-TGG5-1
,
LOC105372878
,
LOC105372879
,
IL19
,
FCMR
,
IL24
,
C1orf116
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48434232
variant
16.

nsv5381285

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DCST1
,
NUDT17
,
THEM5
,
RPS15AP12
,
LOC100271842
,
LOC100216488
,
LOC107985464
,
LOC105371438
,
GORAB
,
B4GALT3
,
SRGAP2D
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
51636542
variant
17.

nsv4685577

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SEPTIN14P12
,
LINC02602
,
PM20D1
,
UTP25
,
MIR4735
,
HSPE1P6
,
TRK-TTT3-1
,
RPL21P19
,
KCNH1
,
LINC01698
,
LOC105371692
,
See more...
Location information:
Clinical significance:
not provided
ID:
50290112
variant
18.

nsv7095569

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRK-TTT8-1
,
ADIPOR1
,
IL10
,
MIR6740
,
LOC105372873
,
MGAT4FP
,
CR1L
,
CBX1P3
,
LARP7P1
,
LOC100420338
,
GOLT1A
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
55275758
variant
19.

nsv4452160

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDCA4P4
,
LOC105372889
,
RPL13AP8
,
TFDP1P1
,
EIF2D
,
CR1
,
LINC02773
,
FDPSP8
,
MAPKAPK2
,
HHAT
,
RPS26P13
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49617795
variant
20.

nsv6310745

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PFKFB2
,
LOC105372878
,
MIR29B2
,
CDCA4P3
,
TRP-TGG5-1
,
IL20
,
LOC105372884
,
LOC105372887
,
IL19
,
MIR29B2CHG
,
IL10
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53674616
variant
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