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Items: 10

2.

nsv3903684

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR3185
,
YWHAEP6
,
RN7SL79P
,
ALOX12-AS1
,
MIEN1
,
ALOXE3
,
KIF18B
,
GPATCH8
,
LOC105371551
,
BCL6B
,
LOC101060400
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467039
variant
3.

nsv3899740

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
P4HB
,
LOC105371808
,
CCT6B
,
TBC1D3F
,
NPEPPS
,
FAM106C
,
ACACA
,
C1QL1
,
MYOCD-AS1
,
MTVR2
,
NFE2L3P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463095
variant
4.

nsv3906245

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR21
,
LOC105371899
,
KRT20
,
KRTAP1-4
,
RPL36AP46
,
LOC105371796
,
NCOR1
,
SAMD11P1
,
ST6GALNAC2
,
STX8
,
LASP1NB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469600
variant
5.

nsv3907261

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SMURF2
,
LOC112268199
,
KLHL11
,
RPS2P46
,
SMYD4
,
LOC107985000
,
STAT5B
,
LOC107985086
,
LOC100420853
,
MTCO3P13
,
LOC105371739
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470616
variant
6.

nsv3914783

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105371922
,
GJD3
,
LOC101930665
,
KRT15
,
HEXIM2
,
NUDT15P2
,
LHX1
,
LOC107985035
,
DUSP3
,
LINC01476
,
RPL36AP46
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478138
variant
7.

nsv4457831

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105371753
,
TAOK1
,
SLFN13
,
LOC105371756
,
LOC102724517
,
LIG3
,
LOC101929494
,
LYRM9
,
TRC-GCA14-1
,
LOC107985055
,
LOC105371750
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49623466
variant
8.

nsv3899598

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RDM1
,
LRRC37A8P
,
LOC105371745
,
CCL5
,
LOC100133244
,
LRRC37A9P
Location information:
Clinical significance:
Benign
ID:
48462953
variant
10.

nsv3919991

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HEATR9
,
LRRC37A9P
,
CCL5
,
LOC100133244
,
LRRC37A8P
,
RDM1
,
TAF15
,
LOC105371745
,
LOC107985049
Location information:
Clinical significance:
Uncertain significance
ID:
48483346
variant
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