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Items: 1 to 20 of 23

1.

nsv3872106

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KLF15
Location information:
Clinical significance:
Benign
ID:
48435461
variant
2.

nsv3873138

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KLF15
Location information:
Clinical significance:
Benign
ID:
48436493
variant
3.

nsv3918094

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
QTRT2
,
MIR544B
,
LSAMP
,
B4GALT4-AS1
,
PRR20G
,
C3orf22
,
KALRN
,
TXNRD3
,
B4GALT4
,
STXBP5L
,
LINC00903
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481449
variant
4.

nsv6311770

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HNRNPA1P23
,
MIX23
,
SLC49A4
,
RAB7A
,
MARK2P6
,
DNAJB6P7
,
LOC90246
,
LOC105374115
,
ROPN1B
,
PRR23E
,
GOLGB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53675641
variant
5.

nsv6112688

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
MTCO1P29
,
PDIA5
,
RNU6-143P
,
LOC112267908
,
OR7E130P
,
PARP9
,
NUP210P1
,
DUTP1
,
KLF15
,
DNAJB8
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150533
variant
6.

nsv3924082

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MYLK-AS2
,
RPL7AP11
,
ALDH1L1-AS2
,
MTCO2P29
,
NAP1L1P3
,
SNRPCP11
,
RPL7P15
,
ZXDC
,
SEC22A
,
NR1I2
,
HACD2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48487437
variant
7.

nsv6112709

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E97P
,
MARK3P3
,
CFAP100-DT
,
LINC01565
,
LOC100419966
,
LOC102723696
,
MUC13
,
MIR5002
,
RHO
,
MBD4
,
PRR23E2P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150554
variant
9.

nsv3885606

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU4-62P
,
SEMA3B-AS1
,
TPRG1
,
ITPR1-DT
,
LOC107986112
,
H3P12
,
NT5DC2
,
OR7E122P
,
SRGAP3
,
C3orf36
,
LOC105377018
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448961
variant
10.

nsv3889228

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB4
,
LOC105374108
,
RPL6P7
,
RNY3P13
,
LINC00960
,
LOC107986110
,
TRH
,
LINC02016
,
LOC105377125
,
ZNF589
,
P2RY1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48452583
variant
11.

nsv3880617

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL23AP49
,
DLEC1
,
TFDP2
,
IGF2BP2
,
BTD
,
RBM5-AS1
,
RAB43
,
FANCD2
,
CYB561D2
,
PFN2
,
GPR149
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48443972
variant
12.

nsv3918981

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02614
,
LINC02054
,
RNU6-143P
,
SEC62
,
MTCH2P1
,
LOC105374144
,
LOC105374041
,
SLC35G2
,
LOC105374147
,
RAP1BP2
,
LINC01998
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482336
variant
13.

nsv6637156

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H1-10
,
AADACL2-AS1
,
PHF5AP7
,
LINC02014
,
LOC105374211
,
PPM1L
,
CEP70
,
SLC9A9
,
OTOL1
,
LOC105374128
,
CRADDP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355985
variant
14.

nsv3922717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR7E53P
,
HSPA8P9
,
H3P12
,
RPS3AP14
,
OR5AC4P
,
RAD51AP1P1
,
ITGB5
,
ZBTB20-AS1
,
RLIG1P2
,
COL6A6
,
CHST2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486072
variant
16.

nsv4673909

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105374083
,
RNU1-30P
,
ALDH1L1-AS2
,
KLF15
,
LOC105374088
,
ALDH1L1
,
LOC107986124
,
ALDH1L1-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
50270734
variant
17.

nsv3920834

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NCK1-DT
,
LOC107986126
,
CRIPTOP6
,
COPB2-DT
,
NUP210P1
,
RNU1-30P
,
FAM86HP
,
GATA2
,
RNU6-789P
,
KBTBD12
,
LINC02021
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48484189
variant
19.

nsv6315343

ID:
53680290
variant
20.

nsv4454406

ID:
49620041
variant
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