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Items: 1 to 20 of 31

1.

nsv3877767

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CYTIP
,
FAM133DP
,
ERMN
Location information:
Clinical significance:
Likely benign
ID:
48441122
variant
2.

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
3.

nsv3898306

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS3AP13
,
LY75-CD302
,
RNU6-546P
,
RPLP0P7
,
GCG
,
RNU6-601P
,
PTP4A1P1
,
LOC105373680
,
FABP5P10
,
MMADHC-DT
,
RPL7P61
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461661
variant
14.

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
15.

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
16.

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
17.

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
18.

nsv3875392

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR10B
,
SCN7A
,
PLA2R1
,
MIR6888
,
LINC01876
,
LOC102724058
,
RAPGEF4-AS1
,
RPL30P2
,
SCN2A
,
CYB5AP2
,
TRA-CGC3-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438747
variant
19.

nsv3874278

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985957
,
LOC101927073
,
LOC105373715
,
LOC105369143
,
CYP2C56P
,
LOC105373712
,
LOC105373709
,
HOXD11
,
PTP4A1P1
,
PPIAP66
,
TANC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48437633
variant
20.

nsv3893853

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SCN7A
,
HEBP2P1
,
SCN9A
,
LOC107985958
,
LOC105373742
,
DLX2-DT
,
LOC100420002
,
RNU6-182P
,
GPD2
,
COBLL1
,
RNA5SP107
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457208
variant
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