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Items: 1 to 20 of 212

1.

nsv6315089

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRKX
,
LOC389906
,
RPS27AP20
Location information:
Clinical significance:
not provided
ID:
53679495
variant
2.

nsv3904162

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NANOGNBP3
,
PRXL2CP1
,
EEF1A1P15
,
P2RY4
,
USP27X-DT
,
NAP1L4P2
,
ARHGAP4
,
TM9SF5P
,
CXorf58
,
DANT2
,
TTC3P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467517
variant
3.

nsv3913255

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NHS-AS1
,
DUSP21
,
ARL5AP5
,
GLOD5
,
ZNF81
,
LOC105373177
,
MIRLET7F2
,
LOC105373386
,
GAGE12D
,
PAGE4
,
CAPN6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476610
variant
4.

nsv3907094

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPR119
,
RN7SKP81
,
PLXNA3
,
RAB40AL
,
EFNB1
,
CT45A6
,
ZNF275
,
CYTH1P1
,
PLS3-AS1
,
MDH1P1
,
PRPF4BP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470449
variant
5.

nsv3878553

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
H2AB2
,
RTL3
,
LOC100419908
,
RNU6-146P
,
ASMTL
,
RNU6-995P
,
ETDB
,
KCTD9P2
,
FIRRE
,
IKBKG
,
TUSC2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48441908
variant
6.

nsv3898149

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
OR3B1P
,
SSX4B
,
ATP6AP1
,
PHF10P1
,
F8
,
LOC105373379
,
RDXP2
,
MID1
,
MIR500B
,
CA5BP1-CA5B
,
ZFP92
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461504
variant
7.

nsv3877395

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ARMCX2
,
RNA5SP505
,
LOC100288233
,
LOC107985645
,
NDUFA5P7
,
CSGALNACT2P2
,
CDR1
,
SRIP2
,
LOC100420089
,
RBM22P7
,
HNRNPH2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440750
variant
8.

nsv3884935

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB11
,
VN1R110P
,
MTND2P25
,
MIR3672
,
GAGE12B
,
RPS7P12
,
STAG2
,
CT45A6
,
OR13H1
,
CTPS2
,
CBLL2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448290
variant
9.

nsv3903061

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC38A5
,
CT45A1
,
INTS6L
,
LOC105373193
,
SKP2P1
,
LOC105373296
,
LOC105377212
,
SERPINA7
,
HNRNPA1P28
,
XAGE2
,
LOC105373299
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466416
variant
10.

nsv3885865

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR1277
,
LOC100420247
,
GAPDHP1
,
EEF1GP5
,
RBMX
,
HDX
,
LOC105373180
,
TCEAL9
,
LOC645188
,
RNA5SP524
,
NHS-AS1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48449220
variant
11.

nsv6112690

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105373176
,
ZFX-AS1
,
LOC101928833
,
ABCB7
,
MTND1P33
,
IKBKGP1
,
TKTL1
,
CT47A4
,
H2BP8
,
MGAT2P1
,
MIR4770
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53150535
variant
12.

nsv3907545

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMEM30BP1
,
SPANXB1
,
SH2D1A
,
LOC107985635
,
RNU6-133P
,
PCNAP3
,
EDA2R
,
SMIM10L2B
,
CLIC4P3
,
ASS1P5
,
AKR7A2P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470900
variant
13.

nsv3884029

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SSX4B
,
LOC100420083
,
CT45A2
,
RNU6-587P
,
CAPZA1P1
,
ATP6AP1
,
GRIPAP1
,
SLC9A7
,
GDI1
,
PHF10P1
,
CYBB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447384
variant
14.

nsv3898185

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ANKRD11P2
,
RAI2
,
ETS2P1
,
RPL6P30
,
GNG5B
,
RPL7P57
,
EEDP1
,
HNRNPH2
,
LOC107987334
,
LOC107987331
,
RNU7-37P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461540
variant
15.

nsv3891981

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PAICSP7
,
RNU6-1323P
,
NUDT11
,
LINC03112
,
MIR424
,
MIR384
,
RPSAP63
,
MIR514A1
,
FAM236A
,
PIN4
,
MIR1298
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455336
variant
16.

nsv3892026

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR934
,
BEX5
,
NFYCP1
,
SHISA5P1
,
PRRG3
,
LOC791092
,
MAMLD1
,
USP11
,
APEX2
,
SH3BGRL
,
SCML1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48455381
variant
17.

nsv3903163

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL36A
,
HMGN1P37
,
ZFP92
,
FTH1P29
,
MIR664B
,
PIGA
,
HSPA8P7
,
RPL39
,
GPRASP3
,
MAGED2
,
LOC105379413
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466518
variant
18.

nsv3887722

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CT45A3
,
MIR503
,
HDAC6
,
FAM9C
,
MPP1
,
SPANXN5
,
LOC107985709
,
POU3F4
,
PAFAH1B2P1
,
MORF4L1P5
,
MAGIX
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48451077
variant
19.

nsv3901047

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPR119
,
BCAP31
,
CXorf38
,
GEMIN8
,
KLHL4
,
RNU7-68P
,
SUPT20HL1
,
IGBP1
,
LOC100422209
,
LOC101928437
,
MTND2P2
,
See more...
Location information:
Clinical significance:
Pathogenic,
conflicting data from submitters
ID:
48464402
variant
20.

nsv3890023

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIRLET7F2
,
TCP11X2
,
ASMT
,
RNA5SP503
,
MIR6089
,
SERBP1P1
,
LOC101928359
,
PJA1
,
PAGE4
,
GYG2
,
LOC105373386
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48453378
variant
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