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Items: 20

1.

nsv7097083

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNQ5
Location information:
Clinical significance:
Uncertain significance
ID:
55277272
variant
2.

nsv4676043

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KNOP1P4
,
LOC105377855
,
KCNQ5-IT1
,
MIR4282
,
KCNQ5
Location information:
Clinical significance:
Uncertain significance
ID:
50272868
variant
3.

nsv3924180

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377875
,
KCNQ5-IT1
,
MIR4463
,
H3P27
,
SLC25A6P6
,
NGRNP2
,
LOC100418957
,
COL12A1
,
LOC105377855
,
RPL39P3
,
LYPLA1P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487535
variant
4.

nsv6315402

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377841
,
RPS6P8
,
LOC105377861
,
LOC105377864
,
LOC642590
,
LOC100419882
,
MIR4282
,
IRAK1BP1
,
RPL37P15
,
RNA5SP209
,
RNU6-280P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680349
variant
9.

nsv5673923

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100422453
,
RPS27P15
,
DDX43
,
MIR4282
,
RNU6-975P
,
RPS6P8
,
SDCBP2P1
,
KHDC1
,
RPL39P3
,
KHDC1L
,
EIF3EP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
52235058
variant
10.

nsv3877040

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378061
,
MIR4640
,
FUCA2
,
TRV-CAC9-1
,
MRPL35P1
,
SFT2D1
,
PLN
,
EIF3EP1
,
EEF1E1
,
LOC105375018
,
MTRF1L
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440395
variant
11.

nsv3879811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-411P
,
LOC107986611
,
RPL5P18
,
MIR1273C
,
TRQ-TTG3-2
,
BVES
,
RPL12P23
,
LOC100421330
,
LOC105378095
,
OR14J1
,
TRA-TGC6-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443166
variant
12.

nsv3887898

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SOD1P1
,
HLA-DPB1
,
H2AC8
,
RNY3P15
,
FBXO30
,
ZDHHC14
,
LOC105378104
,
ZNF76
,
LOC100507547
,
IL17F
,
SLC35D3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451253
variant
13.

nsv3889814

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ITPR3
,
HSD17B8
,
TRAM2-AS1
,
RPL12P23
,
LOC100132834
,
LOC105374869
,
MIR548AJ1
,
H2BC4
,
OR2J2
,
BTF3P7
,
TRA-AGC23-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453169
variant
14.

nsv4350067

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HLA-DPB2
,
CIMIP3
,
LY6G5B
,
MEP1A
,
CILK1
,
NCR2
,
SKIC2
,
SNORD52
,
COL19A1
,
CLNS1AP1
,
HLA-DQB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344980
variant
15.

nsv6313857

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928570
,
RNU4-72P
,
RNA5SP210
,
LOC100422453
,
PIMREGP3
,
TMEM30A-DT
,
DOP1A
,
BECN1P2
,
COX7A2
,
LOC105377891
,
HTR1B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677728
variant
16.

nsv6637121

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNQ5
,
LOC643067
,
KCNQ5-DT
,
RIMS1
,
LOC100418957
,
LOC100422453
,
KCNQ5-IT1
,
LOC107986611
Location information:
Clinical significance:
Uncertain significance
ID:
54355950
variant
17.

nsv7097082

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC643067
,
KCNQ5
,
KCNQ5-DT
,
RIMS1
,
LOC100418957
,
LOC100422453
,
LOC107986611
Location information:
Clinical significance:
Uncertain significance
ID:
55277271
variant
18.

nsv3911444

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KNOP1P4
,
KCNQ5
,
PGAM1P10
,
KCNQ5-AS1
,
KHDC1P1
,
KHDC1L
,
RBPMS2P1
Location information:
Clinical significance:
Uncertain significance
ID:
48474799
variant
19.

nsv6312591

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNQ5
,
DPPA5
,
RN7SL827P
,
OOEP
,
EIF3EP1
,
KHDC1
,
SDCBP2P1
,
RPL39P3
,
KHDC1L
,
RPS6P8
,
RNU6-975P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
53676462
variant
20.

nsv4675253

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KCNQ5
,
OOEP
,
DPPA5
,
EIF3EP1
,
KHDC1L
,
SDCBP2P1
,
RPL39P3
,
KHDC1
,
KHDC1P1
,
CGAS
,
RPSAP41
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
50272078
variant
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