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Items: 13

2.

nsv3883608

ID:
48446963
variant
3.

nsv3877365

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MARK1
,
LINC02766
,
FDPS
,
PRUNE1
,
GJB4
,
RN7SL653P
,
PPIEL
,
CRB1
,
SELENBP1
,
LBR
,
CHML
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48440720
variant
4.

nsv3885206

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SNAP47
,
STK40
,
RNU6-750P
,
LINC01138
,
MIR4632
,
LOC107985100
,
EIF2D
,
SEPTIN7P13
,
RAB13
,
LOC107985524
,
DR1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48448561
variant
5.

nsv3884414

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU1-153P
,
MIR3917
,
LOC105378793
,
CCDC190
,
RPL29P6
,
RUNX3-AS1
,
MIXL1
,
LCE1B
,
NAXE
,
PDC-AS1
,
BNIPL
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48447769
variant
6.

nsv3901163

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TMEM222
,
ZBTB8OS
,
AHDC1
,
HSPE1P8
,
RPL32P6
,
LINC01685
,
GJA9-MYCBP
,
LOC105378662
,
IFITM3P7
,
GJB4
,
TRIM62
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48464518
variant
7.

nsv6313688

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107984940
,
PPIAP36
,
AIRIM
,
EFCAB14P1
,
RPS29P6
,
LOC100328982
,
SLC6A9
,
NFYC-AS1
,
RNA5SP47
,
SMAP2
,
GJB5
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677559
variant
8.

nsv3874782

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929444
,
GJB4
,
EVA1B
,
ZBTB8OS
,
OSCP1
,
CSMD2-AS1
,
FAM229A
,
AGO3
,
EEF1A1P46
,
C1orf216
,
TMEM35B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48438137
variant
9.

nsv3893192

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
COL8A2
,
CSF3R
,
GRIK3
,
THRAP3
,
TRAPPC3
,
TEKT2
,
ADPRS
,
EVA1B
,
MAP7D1
,
MRPS15
,
SH3D21
,
See more...
Location information:
Clinical significance:
Likely pathogenic
ID:
48456547
variant
11.

nsv4436181

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC01776
,
IGSF21-AS1
,
BRI3P1
,
LINC01635
,
ACOT11
,
RPL23AP17
,
NFYC
,
RPL7L1P22
,
EPHA2-AS1
,
SH3BGRL3
,
ECE1-AS1
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49579785
variant
12.

nsv3878135

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC02786
,
LOC105378678
,
CFAP144
,
TLR12P
,
B4GALT2
,
ST3GAL3-AS1
,
AKR1A1
,
ZSCAN20
,
FHL3
,
PPT1
,
RNU6-605P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
48441490
variant
13.

nsv4450729

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
UBE2V2P4
,
LOC100128093
,
TRAPPC3
,
AGO3
,
EVA1B
,
TEKT2
,
MAP7D1
,
THRAP3
,
ADPRS
,
COL8A2
,
RN7SL131P
,
See more...
Location information:
Clinical significance:
Uncertain significance
ID:
49616364
variant
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