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Items: 13

1.

nsv4457531

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ATP13A1
,
PBX4
,
GMIP
,
ZNF101
,
LPAR2
Location information:
Clinical significance:
Uncertain significance
ID:
49623166
variant
2.

nsv3904885

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF321P
,
ZNF861P
,
ZNF816
,
ARID3A
,
MIR642B
,
LOC105372295
,
LOC105372424
,
PTOV1-AS2
,
SLC8A2
,
LOC105372401
,
ZNF419
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468240
variant
3.

nsv3903203

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BABAM1
,
BEST2
,
CALR3
,
SNAR-A8
,
RFPL4AP1
,
RPL39P35
,
OSTCP3
,
LOC105372291
,
SLC25A36P1
,
ZNF653
,
SCN1B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466558
variant
4.

nsv3903092

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LENG8
,
SYDE1
,
FBN3
,
ZNF419
,
ZNF793
,
RNU4-60P
,
LOC105372420
,
NAPSA
,
CARM1
,
KEAP1
,
ZNF14
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466447
variant
5.

nsv3913730

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BCKDHA
,
ADGRE5
,
CLEC17A
,
VN1R83P
,
SNORA68B
,
LOC105372370
,
MAN2B1
,
PGK1P2
,
AKAP8L
,
ZNF567-DT
,
CC2D1A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477085
variant
6.

nsv6290300

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF420
,
LOC105372330
,
BNIP3P31
,
LOC105372353
,
RPL36AP51
,
RN7SL491P
,
SCGB2B2
,
ZNF676
,
SNX6P1
,
ZNF565
,
IFNL2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53634177
variant
7.

nsv3914228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372355
,
SUGP2
,
PLVAP
,
NUDT19
,
LOC105372335
,
CEBPA-DT
,
LOC105372358
,
LOC105372332
,
MIR1270
,
LOC105372361
,
UPF1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477583
variant
8.

nsv3922457

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
REX1BD
,
ZNF92P2
,
LOC105376917
,
LOC100421620
,
LOC105372300
,
LOC105372323
,
BNIP3P33
,
LOC100131479
,
ZNF726
,
RAB3A
,
BNIP3P29
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485812
variant
9.

nsv3921076

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MRPL34
,
BNIP3P25
,
LOC105372298
,
GDF15
,
BNIP3P17
,
OR10H2
,
ZNF676
,
B3GNT3
,
ZNF729
,
BNIP3P31
,
MPV17L2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484431
variant
10.

nsv3895942

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BNIP3P37
,
ZNF675
,
ELL
,
ANO8
,
LOC100533638
,
BORCS8
,
FCHO1
,
LOC100418991
,
RNA5SP468
,
ZNF43
,
FKBP8
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459297
variant
11.

nsv4729750

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105372309
,
RAB8A
,
CYP4F10P
,
TMEM161A
,
MIR1470
,
PGLS-DT
,
IL12RB1
,
LSM4
,
NDUFA13
,
GMIP
,
CYP4F24P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50373387
variant
12.

nsv4457826

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF56P
,
YJEFN3
,
ZNF14
,
LOC101060187
,
ATP13A1
,
PBX4
,
CILP2
,
NDUFA13
,
PHF5AP1
,
TSSK6
,
ZNF101
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49623461
variant
13.

nsv4436023

Variant type:
complex substitution
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NCAN
,
BORCS8-MEF2B
,
ZNF14
,
ZNF708
,
ZNF43
,
ZNF56P
,
ZNF66
,
ZNF726P1
,
ZNF85
,
ZNF90
,
ZNF91
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49579627
variant
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