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Items: 1 to 20 of 59

1.

nsv3895071

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL10AP1
,
MARK3
Location information:
Clinical significance:
Benign
ID:
48458426
variant
2.

nsv3914561

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR889
,
GLRX5
,
RPSAP5
,
MIR5195
,
RPL13P6
,
CLBA1
,
CRIP2
,
IGHVII-43-1
,
LOC105370661
,
MIR1185-1
,
BDKRB2
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477916
variant
3.

nsv4684265

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB3P4
,
LINC02320
,
PACS2
,
EXOC3L4
,
SNORD114-29
,
MIR8071-1
,
IGHV3-50
,
BEGAIN
,
MIR433
,
LOC105370656
,
MTA1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50287388
variant
4.

nsv3911746

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MIR1185-2
,
LOC105370685
,
RPS26P49
,
IGHV3-30
,
TEX22
,
MIR2392
,
SNORD114-15
,
RPL21P13
,
IGHJ1P
,
MIR377
,
RAP2CP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475101
variant
5.

nsv3921506

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL21P13
,
EXOC3L4
,
SNORD114-29
,
MIR8071-2
,
SNORD113-7
,
MIR889
,
IGHV3-65
,
BEGAIN
,
MIR134
,
SNORD114-12
,
IGHV3-62
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48484861
variant
6.

nsv3902723

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
NDUFB3P4
,
TDRD9
,
COA8
,
BEGAIN
,
LOC105370673
,
LINC02298
,
INF2
,
CEND1P1
,
PACS2
,
SNORD114-12
,
LINC02320
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48466078
variant
7.

nsv3922827

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RNU6-1316P
,
MIR136
,
IGHV1-12
,
IGHVIII-67-2
,
MIR654
,
RTL1
,
IGHVII-46-1
,
IGHV3-15
,
LINC02285
,
MARK3
,
RN7SL634P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48486182
variant
8.

nsv3914191

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHV4-55
,
MIR134
,
CEP170B
,
DYNC1H1
,
IGHD3-10
,
IGHJ5
,
LINC02320
,
SNORD114-29
,
SNORD113-7
,
LINC02298
,
LOC105378184
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48477546
variant
9.

nsv3918080

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPR132
,
IGHV3-23
,
MIR300
,
MIR380
,
IGHV3-54
,
IGHM
,
LOC105370673
,
IGHV1-68
,
ANKRD9
,
LOC105378184
,
GOLGA4P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481435
variant
10.

nsv6314048

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHD4-23
,
XRCC3
,
IGHD5-18
,
IGHV5-78
,
ZFYVE21
,
IGHV3-11
,
IGHVII-49-1
,
IGHV3-42
,
IGHVIII-47-1
,
IGHV1-14
,
RPL13P6
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
53677919
variant
11.

nsv4456944

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHV1-58
,
IGHVII-60-1
,
RPL17P4
,
IGHV1-24
,
IGHD1-20
,
IGHV3-16
,
IGH
,
IGHV4-4
,
MIR6765
,
IGHD1-1
,
IGHD5-18
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49622579
variant
12.

nsv3917997

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHV3-23
,
IGHV3-54
,
IGHVII-15-1
,
IGHV1-68
,
IGHV3-69-1
,
IGHVII-65-1
,
IGHD6-25
,
IGHD2-2
,
IGHM
,
IGHV1-46
,
IGHJ1P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481352
variant
13.

nsv3917679

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LINC00221
,
BRF1
,
IGHV1-18
,
IGHV3-23
,
IGHVIII-76-1
,
IGHD2-2
,
IGHV1-68
,
PPP1R13B-DT
,
IGHV3-20
,
TEX22
,
SIVA1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481034
variant
14.

nsv4729218

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHV4-61
,
IGHD3-9
,
IGHV4-39
,
IGHD3-22
,
IGHV3-33
,
IGHVIII-25-1
,
IGHJ4
,
RPS2P4
,
IGHD4-17
,
IGHV2-5
,
LINC02280
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
50372855
variant
15.

nsv3893817

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
MOK
,
LINC02691
,
IGHV1-58
,
IGHD7-27
,
LOC102723342
,
LINC02323
,
ASPG
,
MIR6765
,
BAG5
,
IGHD1-20
,
LINC00226
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48457172
variant
16.

nsv3914922

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
GPR132
,
IGHD5-18
,
CINP
,
LOC107987209
,
MIR12121
,
GOLGA4P1
,
IGHD4-23
,
IGHV3-72
,
CDC42BPB
,
IGHV5-78
,
IGHEP1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48478277
variant
17.

nsv7148227

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
TNFAIP2
,
IGHV4-30-2
,
IGHV4-34
,
HOMER2P2
,
IGHV3-25
,
IGHVII-67-1
,
IGHD3-3
,
RNU4-68P
,
IGHV1-69
,
RNU7-160P
,
IGHV7-81
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
55378143
variant
19.

nsv4456320

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC105378184
,
LINC02298
,
CDC42BPB
,
MIR12121
,
CEP170B
,
ANKRD9
,
COA8
,
GPR132
,
EXOC3L4
,
LOC107984670
,
GOLGA4P1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
49621955
variant
20.

nsv3918299

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
IGHVII-30-1
,
IGHJ4
,
IGHG3
,
RAP2CP1
,
IGHV3-64
,
IGHV2-5
,
LOC107984648
,
LINC02280
,
IGHGP
,
IGHV4-39
,
IGHVIII-13-1
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48481654
variant
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