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Items: 1 to 20 of 40

1.

nsv3904789

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RALYL
Location information:
Clinical significance:
Benign
ID:
48468144
variant
2.

nsv3905893

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RALYL
,
RNU6-1040P
Location information:
Clinical significance:
Benign
ID:
48469248
variant
3.

nsv3912264

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RALYL
,
LOC101929943
,
TPM3P3
Location information:
Clinical significance:
Uncertain significance
ID:
48475619
variant
4.

nsv3911034

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375933
,
LOC105375930
,
MIOXP1
,
LOC107986893
,
REXO1L4P
,
LOC107986896
,
LOC107986953
,
REXO1L9P
,
LOC107986956
,
LOC105375913
,
RIPK2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474389
variant
5.

nsv3914059

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL107P
,
COX6B1P6
,
SNX16
,
CNBD1
,
SLC10A5
,
IL7
,
LOC100533622
,
PARAIL
,
ZNF704
,
RPL3P9
,
LOC105375629
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477414
variant
6.

nsv3922848

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MITA1
,
CA3-AS1
,
RNU6-1220P
,
HIGD1AP6
,
LINC01419
,
HNRNPA1P36
,
LOC105375920
,
MIR5681B
,
CA1
,
TMEM70
,
CRISPLD1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486203
variant
7.

nsv6315163

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF704
,
RN7SL107P
,
C4orf46P3
,
LOC107986953
,
LOC107986893
,
ZFHX4-AS1
,
LINC01607
,
LOC105375924
,
RPL32P4
,
OCIAD2P1
,
SLC25A51P3
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53679673
variant
8.

nsv6313579

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375915
,
LOC105375918
,
CA2
,
RALYL
,
WWP1
,
CNBD1
,
HMGB1P41
,
PKIA
,
HEY1
,
RNU11-6P
,
LINC02605
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677450
variant
9.

nsv3915173

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RN7SL474P
,
UNC5D
,
VN1R45P
,
MIOXP1
,
VIRMA
,
PRDM14
,
LOC100996662
,
ZFAT-AS1
,
C1GALT1P3
,
LOC105375779
,
LOC105375933
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478528
variant
10.

nsv3901821

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TBC1D31
,
LOC105375740
,
ESCO2
,
MIR6847
,
TNFRSF10C
,
RHOBTB2
,
ATP6V1G1P2
,
LOC105375637
,
MTND5P41
,
RNU6-144P
,
MAFA
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48465176
variant
11.

nsv4349554

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929488
,
TEX15
,
LOC105375789
,
MTND4LP26
,
LOC105379384
,
DEFA1B
,
MIR1302-7
,
PTP4A3
,
LOC101927997
,
LINC02990
,
XKR6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49344467
variant
12.

nsv3916777

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL5P22
,
ARHGEF10
,
LOC107986952
,
FAM90A6P
,
LOC105375692
,
EFR3A
,
RNF139
,
NCAPGP1
,
LY6S
,
ZNNT1
,
CYCSP22
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480132
variant
13.

nsv3898123

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPAG1
,
LOC101927657
,
PPIAP84
,
BMP1
,
TUSC3
,
LOC100129098
,
RPL10P18
,
LOC105375873
,
SQLE-DT
,
LOC105375638
,
SIRLNT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48461478
variant
14.

nsv3908608

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01617
,
PENK-AS1
,
RPS2P33
,
IMPDH1P6
,
LOC105375716
,
OR7E157P
,
TRE-CTC14-1
,
PBK
,
MROH4P
,
PDLIM2
,
SNORD65B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48471963
variant
15.

nsv3893757

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105375890
,
TRE-CTC14-1
,
TARDBPP4
,
CYP11B2
,
ZFPM2-AS1
,
IMPDH1P6
,
RNY4P5
,
MIR548H4
,
LOC105379228
,
TMEM68
,
RPS2P33
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457112
variant
16.

nsv3923310

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268023
,
RPL23AP96
,
RN7SL228P
,
RNA5SP272
,
LOC107986976
,
ADCY8
,
MIR6841
,
LOC100422614
,
LY6D
,
LOC105375630
,
RN7SL19P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486665
variant
17.

nsv3914307

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107986897
,
NUGGC
,
TRF-GAA12-1
,
RN7SKP29
,
TMEM74
,
RAD54B
,
CCNE2
,
ATP6V1G1P2
,
RNU6ATAC8P
,
PPP2CB
,
LOC105375785
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477662
variant
18.

nsv3919282

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR4662B
,
LOC101927845
,
PTCSC1
,
LOC105375723
,
RNU1-124P
,
LOC105375932
,
CEBPD
,
OSGIN2
,
EBF2
,
LOC107986938
,
PABPC1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482637
variant
19.

nsv3919200

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268023
,
LOC105375925
,
SDCBP
,
DEFB109C
,
C8orf89
,
LY6S-AS1
,
NRBP2
,
LOC107986954
,
LOC105375630
,
GAPDHP62
,
PIWIL2-DT
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48482555
variant
20.

nsv3906425

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC112268016
,
KIFC2
,
LOC101927513
,
COX6CP8
,
DPYS
,
FZD3
,
MSL3P3
,
FAM135B
,
ENPP2
,
RPS3AP32
,
LOC105375623
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469780
variant
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