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Items: 1 to 20 of 24

1.

nsv3923759

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EREG
,
EFL1P2
,
ST3GAL1P1
,
LOC105377313
,
ANXA3
,
TBCAP3
,
STPG2
,
LOC107986232
,
LOC105377270
,
LOC642474
,
LOC105377273
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487114
variant
2.

nsv4729598

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PTPN11P5
,
LOC643014
,
ANKRD17-DT
,
TECRP1
,
LOC101928893
,
RPS21P3
,
LOC100421494
,
RNU5A-2P
,
COQ2
,
DCK
,
LOC105377295
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50373235
variant
3.

nsv6314916

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MICOS10P4
,
SULT1B1
,
LOC105377275
,
SOWAHB
,
EPGN
,
AREG
,
LOC100422021
,
SUMO2P11
,
COX5BP1
,
SNX5P1
,
LOC100422024
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53679190
variant
4.

nsv4674589

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SOWAHB
,
FTLP9
,
AREG
,
MIR4450
,
EPGN
,
LOC105377313
,
RASGEF1B
,
LOC102724916
,
COX5BP1
,
LOC391674
,
ADAMTS3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271414
variant
5.

nsv4674141

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COX18
,
UGT2B11
,
ANKRD17
,
LOC105377299
,
NPFFR2
,
PPEF2
,
LOC107986287
,
LOC101927297
,
RNA5SP163
,
CCDC158
,
LOC105377282
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50270966
variant
6.

nsv3922666

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100421142
,
HIGD1AP13
,
LOC107986294
,
RPS21P3
,
LOC101928893
,
LOC100421494
,
RNU5A-2P
,
GK2
,
RPSAP39
,
SHROOM3-AS1
,
PTPN11P5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486021
variant
9.

nsv3873978

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100422029
,
H2AZ1
,
LOC101928217
,
LINC02435
,
RHOH
,
RNU6-35P
,
DCK
,
CEP44
,
LOC105378242
,
RN7SL492P
,
LOC105374392
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437333
variant
10.

nsv3876533

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100420289
,
LOC100131038
,
HS3ST1
,
UGDH
,
MTATP6P9
,
LOC105377495
,
RNU6-310P
,
TBCK
,
AGA-DT
,
MYL5
,
LOC105377604
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439888
variant
11.

nsv3884499

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTND4LP29
,
RNU6-128P
,
LINC01258
,
LOC101927179
,
LINC02173
,
CTBP1-AS
,
GALNT7-DT
,
LOC391711
,
TBC1D1
,
SUMO2P11
,
RN7SKP235
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447854
variant
12.

nsv3880085

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268460
,
LINC02435
,
MIR576
,
RN7SL492P
,
PRMT5P1
,
DEFB108F
,
LOC100422029
,
USP17L24
,
LINC00575
,
TAPT1
,
LINC02503
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443440
variant
13.

nsv3883791

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377343
,
PDGFC
,
LOC105374535
,
RPL7AP29
,
LOC101928893
,
GATB
,
LOC102723704
,
LOC101928658
,
LOC105377558
,
NAAA
,
LOC107986328
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447146
variant
14.

nsv6291432

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNHG27
,
TNIP3
,
KPNA2P1
,
RNU6-699P
,
RNU6-224P
,
LYPLA1P2
,
TMPRSS11A
,
HMGB3P15
,
RNU6-1252P
,
UBE2CP3
,
LINC02485
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53636827
variant
15.

nsv3913811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377297
,
HNRNPA1P56
,
MTCO3P27
,
LOC101928760
,
HSP90AB3P
,
ADGRL3-AS1
,
ADGRL3
,
CXCL13
,
LOC105377294
,
RN7SL822P
,
LOC107986279
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477166
variant
16.

nsv3916323

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UGT2B28
,
HMGA1P2
,
LOC100421141
,
PF4
,
UGT2A1
,
CXCL8
,
RNU6-520P
,
TMSB4XP8
,
GPRIN3
,
CXCL9
,
SPOPLP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479678
variant
17.

nsv6313510

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HIGD1AP13
,
CXCL11
,
LOC105377278
,
ART3
,
BMP3
,
TECRP1
,
RPL30P5
,
RN7SL127P
,
LOC102723338
,
LOC105377306
,
RNU5A-2P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677381
variant
18.

nsv4456913

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KPNA2P1
,
CCNG2
,
LOC100422402
,
CXCL1
,
UGT2B24P
,
FTLP9
,
POLR2MP1
,
UGT2A3
,
UGT2B27P
,
LOC107986292
,
CABS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49622548
variant
19.

nsv3920040

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNORD144
,
HELQ
,
CXCL5
,
SCARB2
,
LOC102724916
,
LOC105377273
,
LOC105377290
,
LOC100526736
,
RASGEF1B
,
HNRNPA3P13
,
AREG
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483395
variant
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