U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 52

1.

nsv6291119

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR548AU
,
PHF2
,
FAM120A
,
LOC100419516
Location information:
Clinical significance:
Uncertain significance
ID:
53636514
variant
2.

nsv3913446

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CUTA
,
SYNGAP1
,
PHF1
Location information:
Clinical significance:
Uncertain significance
ID:
48476801
variant
3.

nsv6315179

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SUGT1P4-STRA6LP
,
NR4A3
,
NUTM2G
,
LOC100132077
,
LOC112268050
,
MFSD14B
,
LOC158435
,
SPTLC1
,
MIR3910-1
,
FYTTD1P1
,
GRIN3A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53679689
variant
4.

nsv4684256

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS26P37
,
MIR27B
,
NAMA
,
MIR3074
,
PTMAP12
,
HSD17B3
,
LOC100132077
,
PLPPR1
,
LOC101928014
,
GRIN3A
,
LOC107987107
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50287379
variant
5.

nsv3922615

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107987097
,
MIR4670
,
RNU6-829P
,
ZNF484
,
MIR24-1
,
NSA2P7
,
LOC643342
,
BEND3P2
,
LOC100507346
,
AOPEP
,
ZNF782
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485970
variant
7.

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
8.

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
9.

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
10.

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
11.

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
12.

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
13.

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
14.

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
15.

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
16.

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
17.

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
18.

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
19.

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
20.

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
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center