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Items: 1 to 20 of 57

1.

nsv4681044

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
50283724
variant
2.

nsv6311284

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
53675155
variant
3.

nsv6311149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
53675020
variant
4.

nsv5381326

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
51636583
variant
5.

nsv6311334

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
53675205
variant
6.

nsv6311148

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
53675019
variant
7.

nsv7095848

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
55276037
variant
8.

nsv7096363

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
Location information:
Clinical significance:
Uncertain significance
ID:
55276552
variant
9.

nsv3889051

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
,
CCDC138
Location information:
Clinical significance:
Benign
ID:
48452406
variant
10.

nsv5564250

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EDAR
,
RANBP2
,
CCDC138
,
RPL39P16
Location information:
Clinical significance:
Uncertain significance
ID:
52011673
variant
11.

nsv3881256

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
EDAR
,
RPL39P16
,
RANBP2
,
CCDC138
Location information:
Clinical significance:
Uncertain significance
ID:
48444611
variant
12.

nsv5381336

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL39P16
,
EDAR
,
RANBP2
,
CCDC138
Location information:
Clinical significance:
Uncertain significance
ID:
51636593
variant
13.

nsv4681091

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL39P16
,
RANBP2
,
EDAR
,
CCDC138
Location information:
Clinical significance:
Uncertain significance
ID:
50283771
variant
14.

nsv4450149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC138
,
RANBP2
,
RPL39P16
,
EDAR
Location information:
Clinical significance:
Uncertain significance
ID:
49615784
variant
15.

nsv7096323

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RANBP2
,
CCDC138
,
EDAR
,
RPL39P16
Location information:
Clinical significance:
Uncertain significance
ID:
55276512
variant
16.

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
17.

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
18.

nsv3872550

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SMIM12P1
,
LIMS4
,
ACTR3
,
LINC02966
,
SRSF3P4
,
NDUFB4P6
,
RPL22P11
,
RPL22P12
,
TTL
,
RPS14P4
,
SLC30A6P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48435905
variant
20.

nsv6313505

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SULT1C3
,
SH3RF3-AS1
,
SNRPGP9
,
RPL39P16
,
GCC2-AS1
,
RPL22P8
,
RGPD4
,
SRSF3P6
,
LINC01594
,
RPL10P5
,
RPL37P12
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677376
variant
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