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Items: 9

1.

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
2.

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
3.

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
4.

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
5.

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
6.

nsv3886123

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FHL3
,
DNALI1
,
LOC105378649
,
GNL2
,
MIR3659
,
SNIP1
,
LOC105378651
,
RPS29P6
,
MTF1
,
CDCA8
,
LOC100129497
,
See more...
Location information:
Clinical significance:
Likely benign
ID:
48449478
variant
8.

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
9.

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
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