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Items: 1 to 20 of 27

1.

nsv3910630

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DAZAP2P1
,
RPL36AP16
,
TRIM51JP
,
LOC105373608
,
LOC105373903
,
LOC105374690
,
C2orf81
,
LOC105377627
,
LOC105373714
,
C2orf78
,
ELF2P4
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473985
variant
2.

nsv6634330

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYP1B1-AS1
,
LOC107985771
,
C2orf15
,
APPAT
,
LINC01799
,
PNO1
,
CENPO
,
LOC102724744
,
RN7SL470P
,
TRQ-TTG5-1
,
LOC105374831
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54348633
variant
4.

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
5.

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
6.

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
7.

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
8.

nsv3876227

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-8P
,
RN7SL313P
,
ANAPC1
,
ANKRD36C
,
IL1R1
,
TMEM127
,
RPL22P10
,
LOC107985931
,
RALBP1P2
,
STARD7
,
IL1RN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48439582
variant
9.

nsv3902899

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MTCO3P45
,
RPS21P2
,
ZBTB45P1
,
WASF1P1
,
ANKRD39
,
ANKRD36
,
NEURL3
,
GMCL1P2
,
LOC105373504
,
LINC01849
,
RANBP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466254
variant
10.

nsv3877583

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL27AP4
,
SLC9A4
,
PANTR1
,
LOC442028
,
BBIP1P1
,
EIF5B
,
CFAP144P2
,
EEF1A1P12
,
NPAS2-AS1
,
LOC105373506
,
KANSL3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440938
variant
11.

nsv3907326

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL22P11
,
PANTR1
,
MITD1
,
LIPT1
,
GPAA1P1
,
LIMS1
,
EIF5B
,
SMIM12P1
,
CFAP144P2
,
LOC105373549
,
REV1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470681
variant
12.

nsv3894687

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NCK2
,
ACTP1
,
FHL2
,
LINC01789
,
GCC2-AS1
,
LOC102724875
,
ANAPC1P6
,
GCC2
,
LOC100288570
,
CAPZBP1
,
IL18R1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458042
variant
13.

nsv3906499

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373511
,
ANAPC1P6
,
LOC105373508
,
TBC1D8-AS1
,
AHCYP3
,
RPL23AP27
,
LOC105375311
,
RALBP1P2
,
CAPZBP1
,
IL1RL1
,
TMEM182
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469854
variant
14.

nsv6314726

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACTG2
,
ACYP2
,
ADD2
,
ADRA2B
,
BIN1
,
ANXA4
,
ATP1B3P1
,
ATP5F1BP1
,
ATP6V1B1
,
AUP1
,
BCYRN1
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
53678749
variant
17.

nsv3878033

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FHL2
,
POU3F3
,
NCK2
,
TGFBRAP1
,
GPR45
,
MRPS9
,
C2orf49
,
ECRG4
,
LINC01102
,
LINC01114
,
LINC02946
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48441388
variant
18.

nsv3901575

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
POU3F3
,
MRPS9
,
LINC01114
,
HMGB3P11
,
RPL23AP27
,
PANTR1
,
LOC101927383
,
LINC01159
,
MRPS9-AS2
,
LOC105373526
Location information:
Clinical significance:
Likely pathogenic
ID:
48464930
variant
19.

nsv3899945

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373521
,
LOC105373524
,
LINC01103
,
LINC01102
,
LOC101927383
,
LOC100287010
,
LINC01114
,
HMGB3P11
,
AHCYP3
,
LINC01965
,
LOC105373522
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48463300
variant
20.

nsv3884005

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01159
,
LINC01114
,
MRPS9
,
HMGB3P11
,
LINC01918
,
LOC105373527
,
MRPS9-AS2
,
MRPS9-AS1
,
TGFBRAP1
,
GPR45
,
LOC105373526
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48447360
variant
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