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Items: 1 to 20 of 55

1.

nsv3918779

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LRRC26
,
SOCS5P2
,
EXD3
,
CCDC183-AS1
,
FCN2
,
RXRA
,
LOC100418938
,
NCLP1
,
C9orf163
,
COL5A1-AS1
,
LOC105376316
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482134
variant
2.

nsv3891854

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LCN10
,
LINC01502
,
DNLZ
,
LOC101928786
,
SOHLH1
,
LOC101928932
,
MIR7114
,
NACC2
,
PAXX
,
SEC16A
,
PAEP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455209
variant
8.

nsv3912247

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ALOX15P2
,
LOC107987061
,
OR5C1
,
NCLP1
,
FOCAD
,
LOC105375969
,
CDRT15P14
,
TLE4
,
LOC105376184
,
LOC401557
,
LOC105376313
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475602
variant
9.

nsv3890420

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBC1D13
,
LOC105376186
,
ZDHHC21
,
ZYG11AP1
,
GBGT1
,
VN2R7P
,
PARK7P2
,
ORM1
,
FGF7P6
,
LOC105376292
,
RN7SL544P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453775
variant
10.

nsv3905118

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR219A2
,
CLCN3P1
,
RORB-AS1
,
KLHL9
,
KRT18P24
,
POLR1E
,
CARD19
,
RNU6-1293P
,
RPS2P34
,
NR5A1
,
IL9RP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468473
variant
11.

nsv3891842

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR13C1P
,
CDC37L1
,
IGKV1OR-3
,
NDUFB6
,
GXYLT1P6
,
LOC105375957
,
CAVIN4
,
ACTL7A
,
CYP4F25P
,
MIGA2
,
LOC105379807
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455197
variant
12.

nsv3895453

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL19P15
,
SPATA31D5P
,
PTENP1-AS
,
CARNMT1-AS1
,
MIR4667
,
HSPA5
,
LOC105376020
,
XLOC_007697
,
BSPRY
,
MIR4672
,
LOC107987109
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48458808
variant
13.

nsv3900967

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
BANCR
,
SETX
,
FBXW2
,
PTGES
,
OR13C5
,
PTENP1
,
CRAT
,
SLC24A2
,
FAM95C
,
LOC105376184
,
ZNG1A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464322
variant
14.

nsv3907479

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR2AM1P
,
RN7SL565P
,
MIR3689F
,
DOCK8
,
PRSS3
,
MFSD14B
,
MAMDC2-AS1
,
HSPC324
,
COL5A1
,
TMEM203
,
MSANTD3-TMEFF1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470834
variant
15.

nsv3922684

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TDRD7
,
CDK9
,
FOCAD
,
BRD3OS
,
LOC401557
,
ENDOG
,
SPATA31A5
,
LOC105376223
,
EIF1P1
,
LOC107987100
,
KANK1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486039
variant
16.

nsv3919257

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107987031
,
LOC105376234
,
LOC107987134
,
RBM17P3
,
PTRH1
,
CNTFR
,
TLR4
,
LOC107987137
,
RNU6-829P
,
IL6RP1
,
LOC112268055
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482612
variant
17.

nsv3915973

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CTNNAL1
,
QSOX2
,
RN7SL462P
,
STXBP1
,
CENPP
,
HRCT1
,
RNU6-855P
,
FOXE1
,
SPTAN1
,
RPL37P17
,
ELP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48479328
variant
18.

nsv3911025

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RORB-AS1
,
FNBP1
,
POLR1E
,
BTF3P4
,
SPATA31B1P
,
RPS2P34
,
MIR31HG
,
LAGE3P1
,
EBLN3P
,
PKN3
,
STXBP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474380
variant
19.

nsv3921598

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PGAP4
,
ECPAS
,
LOC101929446
,
LOC105376239
,
LOC613206
,
RALGPS1
,
LOC105375959
,
RNU6-492P
,
LOC105376325
,
LMX1B
,
CHCHD4P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484953
variant
20.

nsv4457273

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CDRT15P14
,
MIR548AW
,
LOC642490
,
LOC102724036
,
LOC101929116
,
RPP25L
,
LOC105376184
,
CCDC171
,
LOC105376101
,
SNORD36B
,
FAM120A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49622908
variant
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