U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 16

1.

nsv6637454

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NPM1P45
,
GLP2R
,
GAS7
,
RCVRN
,
GSG1L2
Location information:
Clinical significance:
Uncertain significance
ID:
54356283
variant
2.

nsv4681489

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MYH2
,
MYH1
,
NPM1P45
,
MYH13
,
MYH4
,
LOC107985004
,
MYHAS
,
RPS27AP1
,
GSG1L2
,
GAS7
,
RCVRN
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50284169
variant
3.

nsv3903684

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR3185
,
YWHAEP6
,
RN7SL79P
,
ALOX12-AS1
,
MIEN1
,
ALOXE3
,
KIF18B
,
GPATCH8
,
LOC105371551
,
BCL6B
,
LOC101060400
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467039
variant
4.

nsv3899740

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
P4HB
,
LOC105371808
,
CCT6B
,
TBC1D3F
,
NPEPPS
,
FAM106C
,
ACACA
,
C1QL1
,
MYOCD-AS1
,
MTVR2
,
NFE2L3P2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463095
variant
5.

nsv3906245

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR21
,
LOC105371899
,
KRT20
,
KRTAP1-4
,
RPL36AP46
,
LOC105371796
,
NCOR1
,
SAMD11P1
,
ST6GALNAC2
,
STX8
,
LASP1NB
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48469600
variant
6.

nsv3907261

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SMURF2
,
LOC112268199
,
KLHL11
,
RPS2P46
,
SMYD4
,
LOC107985000
,
STAT5B
,
LOC107985086
,
LOC100420853
,
MTCO3P13
,
LOC105371739
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48470616
variant
7.

nsv3897625

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GP1BA
,
POLR2A
,
TSR1
,
RPS26P53
,
MYH2
,
ALOX12-AS1
,
SPNS2-AS1
,
EMC6
,
SENP3
,
MIR1253
,
GLP2R
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48460980
variant
8.

nsv3915354

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
KIF1C-AS1
,
TMEM107
,
XAF1
,
ACAP1
,
RNASEK
,
OR1A2
,
MINK1
,
GPS2
,
SNORD91A
,
LOC101927864
,
RN7SL601P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478709
variant
9.

nsv3917059

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PSMB6
,
RNU6-1065P
,
ALOX15B
,
RPH3AL
,
SLC25A11
,
EIF4A1
,
TNFSF12-TNFSF13
,
LOC107984988
,
LOC107985011
,
SNORD10
,
MIR4521
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480414
variant
10.

nsv7148254

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RFLNB
,
C17orf100
,
KDM6B
,
TNK1
,
RABEP1
,
UBE2G1
,
LOC105371526
,
MIR22
,
VMO1
,
INCA1
,
PFN1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378170
variant
11.

nsv3904771

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SLC2A4
,
CCDC92B
,
USP43
,
DBIL5P
,
PITPNA
,
LOC105371485
,
METTL16
,
TLCD3A
,
RNF227
,
RNA5SP435
,
OR3A1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48468126
variant
12.

nsv3911050

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
C17orf49
,
SPEM1
,
PHF23
,
LOC107987244
,
CTDNEP1
,
SHISA6
,
MAGOH2P
,
ALOX15P1
,
ATP1B2
,
FBXO39
,
EIF4A1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474405
variant
13.

nsv1398516

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SCO1
,
DNAH9
,
MYH3
,
TMEM220
,
RNU6-1065P
,
GAS7
,
ZNF18
,
TMEM220-AS1
,
GSG1L2
,
RCVRN
,
MYH2
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
30348179
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