U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 128

1.

nsv4729244

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MFHAS1
,
CLDN23
Location information:
Clinical significance:
Uncertain significance
ID:
50372881
variant
2.

nsv3890708

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLDN23
,
LOC105379225
,
RN7SL178P
,
LOC105379224
Location information:
Clinical significance:
Likely benign
ID:
48454063
variant
3.

nsv3897142

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CLDN23
,
LOC105379225
,
RN7SL178P
,
LOC105379224
Location information:
Clinical significance:
Benign
ID:
48460497
variant
4.

nsv6636765

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MFHAS1
,
LOC105379224
,
RN7SL178P
,
LOC105379225
,
CLDN23
Location information:
Clinical significance:
Uncertain significance
ID:
54355594
variant
5.

nsv6315449

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101928016
,
RPL23AP54
,
NAT1
,
LOC102725080
,
FAM90A21P
,
DEFT1P
,
LOC105379289
,
SUB1P1
,
MIR548I3
,
MIR1322
,
DEFB130B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53680396
variant
6.

nsv3917350

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC03022
,
RPS3AP31
,
DEFB134
,
RNU7-153P
,
LOC100421094
,
ATP6V1B2
,
FAM90A14
,
OR7E125P
,
MRPL49P2
,
RPL30P9
,
LOC105379325
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48480705
variant
7.

nsv7148253

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ENTPD4
,
LOC100421446
,
SH2D4A
,
LOC107986919
,
LOC101928095
,
MRPL49P2
,
DEFB103A
,
BMP1
,
RPL23AP96
,
RPL9P20
,
DEFA10P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378169
variant
8.

nsv6636968

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF705B
,
NATP
,
LOC392187
,
MRPS18CP3
,
RPL32P19
,
TRK-TTT17-1
,
MSRA
,
KBTBD11-AS1
,
FAM90A8
,
LOC102723313
,
SPAG11A
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355797
variant
9.

nsv4455719

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR598
,
RPL19P13
,
DEFB135
,
SNRPCP17
,
LOC100421023
,
FAM66B
,
LOC105379220
,
LOC105379237
,
RPS3AP30
,
DEFB131D
,
TRMT9B
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621354
variant
10.

nsv4685988

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ZNF705B
,
RNU6-682P
,
LOC105379237
,
MSRA-DT
,
RNA5SP252
,
MIR4659A
,
DEFT1P2
,
FAM90A8
,
FAM90A3
,
CLN8
,
FAM90A9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50290734
variant
11.

nsv7148131

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
XKR6
,
FAM90A11
,
DEFA7P
,
LOC392180
,
LOC157273
,
DEFA1
,
DEFA5
,
MIR4286
,
ENPP7P1
,
DEFA9P
,
MRPS18CP2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378047
variant
12.

nsv6634376

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DLGAP2-AS1
,
MIR124-1HG
,
KBTBD11-OT1
,
FAM87A
,
RPL17P29
,
FAM90A23
,
MCPH1
,
LOC100420053
,
RNU6-1084P
,
FAM66B
,
LOC401442
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54348679
variant
13.

nsv6636940

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
HSPD1P3
,
LOC401442
,
LOC105377783
,
SUB1P1
,
RPS3AP30
,
RPL23AP54
,
DEFB135
,
FAM90A17
,
LOC105379237
,
DEFB4B
,
FAM86B3P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
54355769
variant
14.

nsv3902717

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC101929128
,
DEFB105B
,
FAM85B
,
LOC107986910
,
PAICSP4
,
PRAG1
,
MIR597
,
SPAG11B
,
LOC112268400
,
LOC105377799
,
MTMR9
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466072
variant
15.

nsv3921576

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
SPAG11B
,
MIR4286
,
DEFB103B
,
ALG1L13P
,
RPL10P19
,
USP17L4
,
PRAG1
,
FAM90A18
,
FAM90A20
,
ZNF596
,
LOC105377781
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484931
variant
16.

nsv3900231

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105377793
,
LOC112268400
,
LOC107986910
,
FAM90A7
,
LOC107986907
,
FAM66E
,
LOC105377796
,
DEFB106A
,
SEPTIN14P8
,
LOC112268397
,
ENPP7P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463586
variant
17.

nsv3911012

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DEFB4A
,
DEFA7P
,
LOC105377790
,
CSMD1
,
LOC392180
,
RNU6-1151P
,
LOC157273
,
LOC105379224
,
PRR23D3P
,
DEFB109B
,
LOC105377784
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48474367
variant
18.

nsv3912676

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
FAM90A23
,
SNRPCP6
,
LOC105379220
,
KBTBD11-OT1
,
SNRPCP17
,
FAM90A4P
,
MCPH1
,
HSPD1P3
,
FAM66B
,
DEFB4B
,
DEFB1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48476031
variant
19.

nsv3900485

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNA5SP251
,
DEFA5
,
LOC101927997
,
FAM90A13
,
FAM90A19
,
PRR23D1
,
PRR23D2
,
LOC157273
,
DEFB4A
,
LOC107986907
,
LOC105377793
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48463840
variant
20.

nsv3903778

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105379230
,
XKR5
,
ERICH1
,
FAM90A20
,
FAM90A18
,
PRR23D2
,
RNA5SP251
,
ZNF596
,
ANGPT2
,
FAM90A15
,
LOC101927997
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48467133
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