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Items: 1 to 20 of 62

1.

nsv3910270

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-71P
,
LINC00676
,
C13orf42
,
LOC105370117
,
MBNL2
,
COMMD6
,
RABEPKP1
,
DCUN1D2
,
LOC105370223
,
RPL31P53
,
VWA8-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473625
variant
2.

nsv3924528

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370271
,
OR7E33P
,
PRELID3BP2
,
LINC00552
,
LOC105370291
,
LOC105370314
,
RPL7L1P6
,
DZIP1
,
LINC00345
,
PRR20A
,
COL4A2-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487883
variant
3.

nsv4675850

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TEX30
,
LOC101927712
,
LINC00676
,
LOC105370246
,
KLF12
,
RPL31P53
,
DCUN1D2
,
COMMD6
,
RNY3P10
,
LOC105370223
,
RABEPKP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272675
variant
4.

nsv3907697

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPC5
,
SNORD31B
,
DPPA3P3
,
PCCA-AS1
,
LOC107984573
,
RNU6-54P
,
TPP2
,
LOC105377815
,
MTND6P37
,
HSP90AB6P
,
SNORA107
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471052
variant
5.

nsv3898603

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNY4P30
,
LOC107987191
,
RNU6-65P
,
GPALPP1
,
LOC105370191
,
LMO7DN-IT1
,
RN7SL413P
,
LOC100129307
,
LINC00459
,
SERPINE3
,
SLAIN1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461958
variant
6.

nsv3918812

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SRSF1P1
,
LOC105370213
,
NDFIP2-AS1
,
ERICH6B
,
LOC105370256
,
LINC00364
,
RN7SKP6
,
NUDT21P1
,
RPS4XP16
,
LOC105370239
,
LINC00560
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482167
variant
7.

nsv6314117

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RBM26
,
RNY4P31
,
MIR4703
,
KBTBD6
,
RPL31P54
,
NEK3
,
DNAJC15
,
LOC105370272
,
RNU6-74P
,
LINC00374
,
BTF3P11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677988
variant
8.

nsv3913649

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL21P108
,
LINC00330
,
FAM124A
,
LOC105370263
,
CBY2
,
PSMC1P13
,
LINC02341
,
RPL35AP31
,
LOC105370174
,
LOC105370220
,
SPRY2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477004
variant
9.

nsv3882264

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARL11
,
RPL18P10
,
LOC105370264
,
RN7SL618P
,
RPS3AP52
,
LOC105370221
,
RNU6-72P
,
LMO7
,
MIR3169
,
LINC00444
,
LINC02338
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48445619
variant
10.

nsv4675995

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU7-88P
,
LINC00564
,
LOC105370292
,
LOC105370269
,
MIR5007
,
LOC105370289
,
SP3P
,
RPL31P54
,
RNY3P10
,
RNU6-81P
,
LOC105370249
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272820
variant
11.

nsv3895373

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00383
,
LOC105370250
,
RPL7L1P1
,
LINC00376
,
LOC105370230
,
ELL2P3
,
RPL21P110
,
LOC102723910
,
TBC1D4
,
LOC105370247
,
LOC105370313
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458728
variant
12.

nsv3915859

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370231
,
RNY1P6
,
LINC02333
,
SERPINE3
,
UCHL3
,
CDADC1
,
SLAIN1
,
KLHL1
,
VPS36
,
SPTLC1P5
,
PHF11
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479214
variant
13.

nsv6291752

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GYG1P2
,
LOC102723968
,
LINC01442
,
LINC00395
,
LOC105370245
,
RNY3P7
,
LOC105370251
,
LOC105370265
,
MTCL1P1
,
RNY1P5
,
LINC00459
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53637147
variant
14.

nsv3913682

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370251
,
MIR548X2
,
LOC105370274
,
LINC00378
,
LOC105370234
,
LINC00358
,
OR7E156P
,
SLAIN1
,
PWWP2AP1
,
LOC100129307
,
CCT5P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477037
variant
15.

nsv3902290

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107987191
,
RNU4-10P
,
PWWP2AP1
,
LMO7DN-IT1
,
LINC00331
,
RAC1P8
,
CCT5P2
,
PTMAP5
,
LINC01078
,
LOC105370234
,
LOC105370274
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465645
variant
16.

nsv3918305

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00397
,
LINC00446
,
RNY3P10
,
LOC105370283
,
COMMD6
,
LOC105370246
,
LOC105370286
,
LOC105370263
,
RPL21P108
,
LINC00392
,
MIR4500
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481660
variant
17.

nsv3895213

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MYCBP2
,
MYCBP2-AS1
,
HNRNPA1P31
,
COMMD6
,
SCEL
,
LOC100288208
,
LINC00402
,
RPS10P21
,
KLF12
,
RPL21P109
,
LOC105370266
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458568
variant
18.

nsv3914942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RIOK3P1
,
MIR3665
,
LMO7DN
,
STARP1
,
LINC02342
,
SRSF1P1
,
LOC107987190
,
LINC00348
,
LINC00364
,
NDFIP2-AS1
,
LOC105370256
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478297
variant
19.

nsv4675244

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-79P
,
LINC01069
,
RN7SL571P
,
LINC00351
,
LOC105370291
,
RNY3P7
,
LOC105370271
,
RPL21P111
,
LINC00561
,
LOC100129307
,
LOC107984620
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272069
variant
20.

nsv3902794

ID:
48466149
variant
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