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Items: 1 to 20 of 71

1.

nsv6636030

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMP20
Location information:
Clinical significance:
Uncertain significance
ID:
54354859
variant
2.

nsv6314513

Variant type:
complex chromosomal rearrangement
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMP25
,
MMP25-AS1
Location information:
Clinical significance:
Uncertain significance
ID:
53678384
variant
3.

nsv3896340

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MMP25-AS1
,
IL32
,
RNU1-125P
,
LOC107984896
,
MMP25
Location information:
Clinical significance:
Benign
ID:
48459695
variant
4.

nsv3896696

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IL32
,
MMP25
,
MMP25-AS1
,
RNU1-125P
Location information:
Clinical significance:
Benign
ID:
48460051
variant
5.

nsv5380796

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FAUP4
,
MMP7
,
SETP17
,
LUZP2
,
MIR6124
,
KCTD9P4
,
CCND1
,
RNU6-1238P
,
RNA5SP339
,
MMP10
,
GPR152
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
51636053
variant
6.

nsv3904761

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPS6P16
,
CTSC
,
LOC105369489
,
RN7SKP273
,
MTCYBP25
,
LOC105369469
,
CCDC81
,
LOC107984388
,
RNU6-560P
,
CASP4LP
,
LOC105369409
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468116
variant
7.

nsv3913977

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PLS1P1
,
SNORA25
,
RPA2P3
,
TAF1D
,
SRP14P2
,
MIR1304
,
LOC105369456
,
MIR4300HG
,
LDHAL6DP
,
TUBAP2
,
LINC02700
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477332
variant
8.

nsv3910101

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PHB1P16
,
LOC100418884
,
LOC101929174
,
SRSF8BP
,
C11orf54
,
SNORD13I
,
LINC02764
,
GRIA4
,
REXO2
,
PPIHP1
,
GPR83
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48473456
variant
9.

nsv6637396

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984375
,
RN7SL222P
,
RPL32P24
,
MMP8
,
BOLA3P1
,
LOC100420800
,
PRSS23
,
PANX1
,
RAB30
,
RAB30-DT
,
HPRT1P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54356225
variant
10.

nsv3894488

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-16P
,
DDX10
,
LOC102723879
,
LOC105369475
,
MAML2
,
MTND1P36
,
MMP12
,
AKTIPP3
,
SLN
,
RNA5SP535
,
LOC105369429
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457843
variant
11.

nsv3910663

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101060084
,
PGAM1P9
,
LOC105369466
,
LOC105369460
,
POGLUT3
,
PGR-AS1
,
CASP4
,
LOC100129203
,
LOC105369463
,
KDM4E
,
LINC02737
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474018
variant
12.

nsv3922508

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
AMOTL1
,
LNCRNA-IUR
,
ANKRD33BP7
,
HIKESHI
,
SNORD5
,
TRIM49D2
,
PRSS23-AS1
,
OR7E13P
,
GRM5-AS1
,
LOC100289416
,
TYR
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48485863
variant
13.

nsv5672640

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPD1P13
,
CARD17P
,
SIK2
,
EXPH5
,
LOC100420803
,
WTAPP1
,
RN7SL222P
,
LOC112268081
,
CYCSP29
,
LOC107984381
,
SMARCE1P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
52233775
variant
17.

nsv6309019

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL21P96
,
RNU6-952P
,
MMP3
,
MMP8
,
MMP12
,
TMEM123-DT
,
MTCO1P15
,
LOC100421658
,
MMP27
,
MMP20
,
RNU7-159P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53672890
variant
19.

nsv3893233

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105376598
,
OSBPL9P2
,
LOC100421985
,
NLRP10
,
GLB1L2
,
LINC02685
,
FTH1P16
,
PTS
,
SORL1-AS1
,
OR9G3P
,
OR8G5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48456588
variant
20.

nsv3900144

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RTN3
,
KRTAP5-13P
,
LOC653503
,
LOC105376646
,
LOC105369539
,
MPPED2
,
DLG2
,
SORL1-AS1
,
YWHABP2
,
SCN3B
,
TRIM53AP
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463499
variant
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