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Items: 1 to 20 of 40

1.

nsv3875272

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
Location information:
Clinical significance:
Likely benign
ID:
48438627
variant
2.

nsv3906919

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
Location information:
Clinical significance:
Benign
ID:
48470274
variant
3.

nsv3893453

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
Location information:
Clinical significance:
Benign
ID:
48456808
variant
4.

nsv3897124

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
Location information:
Clinical significance:
Benign
ID:
48460479
variant
5.

nsv4453943

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
Location information:
Clinical significance:
Uncertain significance
ID:
49619578
variant
6.

nsv3879685

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
,
MIR561
,
RNA5SP114
,
LINC01090
Location information:
Clinical significance:
Benign
ID:
48443040
variant
7.

nsv3889556

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP114
,
GULP1
,
LINC01090
Location information:
Clinical significance:
Benign
ID:
48452911
variant
8.

nsv3917182

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR561
,
LOC729141
,
LINC01090
,
RNA5SP114
,
GULP1
Location information:
Clinical significance:
Uncertain significance
ID:
48480537
variant
9.

nsv6291232

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GULP1
,
RNA5SP114
,
LOC729141
,
MIR561
,
LINC01090
Location information:
Clinical significance:
Uncertain significance
ID:
53636627
variant
10.

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
11.

nsv3894939

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TRE-TTC9-1
,
DNAJC19P5
,
LINC01923
,
RBM45
,
TMEFF2
,
NABP1
,
PJVK
,
LOC107985968
,
LOC107985965
,
CASP10
,
KCTD18
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458294
variant
12.

nsv6315398

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985785
,
MYO1B
,
SF3B1
,
DSTNP5
,
GAPDHP59
,
ZDBF2
,
OSGEPL1-AS1
,
PLEKHM3
,
STK17B
,
NIF3L1
,
LOC105373823
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680345
variant
13.

nsv3899404

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01877
,
MFSD6
,
LOC105373770
,
DIRC1
,
C2orf66
,
LOC105373793
,
CAVIN2-AS1
,
LOC105373796
,
LOC105373833
,
LOC105373836
,
LOC105373816
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48462759
variant
14.

nsv4451512

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01117
,
LOC107985958
,
RNU7-44P
,
RPSAP25
,
RNU6-182P
,
MIR3606
,
DUSP19
,
IFT70B
,
MIR6512
,
PLEKHA3
,
CYB5AP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49617147
variant
15.

nsv4674757

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OSBPL6
,
DNAJC19P5
,
HOXD4
,
LOC102724194
,
LOC107985968
,
LOC105373777
,
LOC105373760
,
NCKAP1
,
LOC102724340
,
LOC105373757
,
HOXD10
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50271582
variant
16.

nsv3895293

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CALCRL-AS1
,
ZC3H15
,
LOC105373766
,
COL5A2
,
HECW2-AS1
,
OSGEPL1-AS1
,
RPL23AP33
,
LOC107985831
,
RPL4P7
,
E2F3P2
,
LOC105373780
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458648
variant
17.

nsv3878976

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FSIP2-AS1
,
LOC105373816
,
LOC105373756
,
KRT18P29
,
DIRC1
,
HIBCH
,
MSTN
,
LOC105373776
,
KRT8P40
,
SLC44A3P1
,
MIR1258
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48442331
variant
18.

nsv3891673

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC729141
,
FTH1P20
,
DLX2
,
RNU7-104P
,
RNU5E-9P
,
H3P7
,
MIR4444-1
,
NFE2L2
,
RN7SKP42
,
RNA5SP112
,
FAM171B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455028
variant
19.

nsv3900193

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OSBPL6
,
LOC105373771
,
NCKAP1
,
MIR3129
,
LOC102724288
,
LOC729254
,
LOC107985785
,
PPP1R1C
,
COL3A1
,
PJVK
,
TMEFF2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463548
variant
20.

nsv3905582

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP35
,
HNRNPA3
,
LOC105373768
,
CALCRL
,
STAT4-AS1
,
RPL27AP3
,
LOC105373785
,
NUP35
,
RPL29P8
,
OSBPL6
,
HAGLR
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468937
variant
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