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Items: 1 to 20 of 107

1.

nsv4456376

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARHGEF7
Location information:
Clinical significance:
Uncertain significance
ID:
49622011
variant
2.

nsv3910270

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-71P
,
LINC00676
,
C13orf42
,
LOC105370117
,
MBNL2
,
COMMD6
,
RABEPKP1
,
DCUN1D2
,
LOC105370223
,
RPL31P53
,
VWA8-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473625
variant
3.

nsv3924528

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370271
,
OR7E33P
,
PRELID3BP2
,
LINC00552
,
LOC105370291
,
LOC105370314
,
RPL7L1P6
,
DZIP1
,
LINC00345
,
PRR20A
,
COL4A2-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487883
variant
4.

nsv4675850

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TEX30
,
LOC101927712
,
LINC00676
,
LOC105370246
,
KLF12
,
RPL31P53
,
DCUN1D2
,
COMMD6
,
RNY3P10
,
LOC105370223
,
RABEPKP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272675
variant
5.

nsv6314171

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4705
,
LOC102724149
,
GAPDHP22
,
KRT18P27
,
L1TD1P1
,
PWWP2AP1
,
LOC105370300
,
CLYBL-AS2
,
LOC105370363
,
TGDS
,
LINC00354
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53678042
variant
6.

nsv3920102

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984609
,
SOX21
,
RPL7L1P6
,
MIR19B1
,
LOC107984566
,
DAOA
,
CARS2
,
LIPT1P1
,
LINC00359
,
TGDS
,
CLCP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48483457
variant
7.

nsv3903376

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZIC2
,
LOC101060553
,
LOC105378193
,
ITGBL1
,
LOC105370384
,
LOC105370324
,
MIR4501
,
MIR8075
,
LOC105370364
,
F10
,
UPF3A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466731
variant
8.

nsv3896487

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMTC4
,
COL4A2
,
PROZ
,
LOC107984574
,
LOC105370365
,
GPR18
,
RASA3
,
EFNB2
,
RNU6-62P
,
NALCN-AS1
,
LOC105370362
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48459842
variant
9.

nsv3890560

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL15P18
,
FGF14-AS1
,
LOC105370364
,
GGACT
,
SLC15A1
,
PCCA-AS1
,
RN7SKP8
,
LINC03032
,
SWINGN
,
ZIC2
,
LOC107987192
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453915
variant
10.

nsv3892450

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS6P23
,
LOC105370344
,
SWINGN
,
LOC105370364
,
ERCC5
,
LOC105370324
,
TM9SF2
,
POGLUT2
,
ZIC2
,
F10
,
LOC105370384
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455805
variant
11.

nsv4675644

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZIC2
,
LINC03032
,
SLC15A1
,
MIR4501
,
GGACT
,
LOC105370364
,
POGLUT2
,
RPL15P18
,
RN7SKP8
,
RPS6P23
,
GRTP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50272469
variant
12.

nsv6637400

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984609
,
LINC00354
,
LOC101927385
,
BIVM
,
LOC107984626
,
CLCP2
,
RPL7L1P6
,
LOC105370360
,
LOC107984566
,
LOC107984606
,
PPIAP24
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356229
variant
13.

nsv6314066

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4502
,
GRTP1-AS1
,
LOC101928730
,
LINC00399
,
RPL35P7
,
LINC00554
,
LDHBP1
,
ABHD13
,
DAOA-AS1
,
ARF4P3
,
RPL35P9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677937
variant
14.

nsv3905010

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SKP10
,
LOC105370362
,
LINC00460
,
ATP11A
,
LOC105370339
,
NALF1
,
LINC00368
,
LINC01070
,
RN7SL783P
,
TEX29
,
LOC107984588
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468365
variant
15.

nsv4728419

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL7P45
,
LOC107984615
,
LOC107984618
,
LOC107984555
,
COL4A1
,
TEX30
,
L1TD1P1
,
LOC101927712
,
RNU1-16P
,
LINC03082
,
TFDP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50372056
variant
16.

nsv3916756

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PROZ
,
LOC105370359
,
RN7SL783P
,
COL4A2
,
COL4A2-AS2
,
DAOA-AS1
,
RASA3
,
EFNB2
,
LINC00460
,
TEX29
,
LOC105370345
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480111
variant
17.

nsv3913569

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TPP2
,
FGF14
,
ARHGEF7
,
SNORD31B
,
LOC107984613
,
LINC00431
,
POGLUT2
,
LOC105370344
,
LOC105370384
,
SWINGN
,
LINC01309
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476924
variant
18.

nsv3905205

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR548AR
,
COL4A2
,
TMEM255B
,
CDC16
,
PROZ
,
MIR8073
,
GAS6
,
LOC105370345
,
COL4A2-AS2
,
ABHD13
,
DAOA-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468560
variant
19.

nsv3922934

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01054
,
SOX1-OT
,
RAB20
,
LOC107984602
,
LOC100506016
,
LINC00368
,
LOC107983958
,
LINC01070
,
CUL4A
,
IRS2
,
LOC112268113
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486289
variant
20.

nsv3905783

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105370372
,
RNA5SP39
,
C13orf46
,
TMCO3
,
LINC00452
,
LINC00567
,
LINC00454
,
LOC102724510
,
LOC107984607
,
LOC107984624
,
LINC00396
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469138
variant
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