222684 AND nstd173 - dbVar

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nsv4383600

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: LOC105371657

Location information:

ID:: 49474333

variant

nsv4387761

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: DMBT1

Location information:

ID:: 49478494

variant

nsv4379109

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: SIRPB1

Location information:

ID:: 49469842

variant

nsv4372435

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: NPEPPSP1

Location information:

ID:: 49463168

variant

nsv4385116

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: ANKRD36B

Location information:

ID:: 49475849

variant

nsv4376456

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: ADAM5; ADAM3A

Location information:

ID:: 49467189

variant

nsv4375271

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: ANKRD36; LOC100506076

Location information:

ID:: 49466004

variant

nsv4372080

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: RPL31P12; LOC105378797

Location information:

ID:: 49462813

variant

nsv4375714

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: UGT2B17; LOC100132651; LOC100422402

Location information:

ID:: 49466447

variant

10.

nsv4367271

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: OR56B2P; OR52N1; OR52N5

Location information:

ID:: 49458004

variant

11.

nsv4384776

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: SIGLEC5; SIGLEC14; RPL7P51

Location information:

ID:: 49475509

variant

12.

nsv4374274

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: TMEM229A; LOC105375483; SPAM1

Location information:

ID:: 49465007

variant

13.

nsv4382082

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: OR4C6; OR4P4; OR4S2; OR4V1P

Location information:

ID:: 49472815

variant

14.

nsv4377819

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: DUSP22

Location information:

ID:: 49468552

variant

15.

nsv4368821

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: LOC391322; GSTTP2; GSTT1; GSTT1-AS1; LOC100420769

Location information:

ID:: 49459554

variant

16.

nsv4378397

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: TAS2R64P; TAS2R43; PRH1-TAS2R14; PRH1; PRH1-PRR4

Location information:

ID:: 49469130

variant

17.

nsv4385187

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Genes(s) in region:: IGHV1-68; GOLGA4P2; LINC00221; IGHVII-53-1; IGHV7-34-1; IGHV5-51; IGHVII-46-1; IGHVIII-13-1; IGHV3-36; IGHVIII-67-2; IGHV1-12; IGHV3-15; IGHV3-41; IGHVII-40-1; IGHV3-64; IGHV1-18; IGHV4-39; IGHV3-20; IGHVIII-44; IGHV1-46; IGHVII-65-1; IGHV3-47; IGHVII-30-1; IGHV4-61; IGHV8-51-1; IGHV3-50; IGHV3-23; IGHV3-33; IGHVIII-25-1; IGHVII-44-2; IGHV1-45; IGHV3-49; IGHV3-22; IGHV3-60; IGHV4-28; IGHVII-30-21; IGHVII-22-1; IGHV3-53; IGHVIII-38-1; IGHV5-10-1; IGHV1-67; IGHVIII-5-1; IGHV3-38; HOMER2P1; IGHV3-29; IGHV3-13; IGHVII-62-1; LOC105370700; IGHVIII-67-4; IGHV7-56; IGHVIV-44-1; IGHVII-67-1; IGHV2-5; IGHVII-51-2; IGHV3-43; IGHV3-19; IGHV3-32; IGHV7-27; IGHV3-66; IGHV1-17; IGHV1-24; IGHVII-60-1; IGHV3-35; IGHV1-58; IGHV4-59; IGHV2-26; LINC00226; IGHV1-69; IGHVIII-11-1; IGHVII-33-1; IGHV3-21; IGHV3-64D; GOLGA4P3; IGHV3-62; IGHV3-48; IGHV7-40; HOMER2P2; IGHVIII-67-3; IGHV3-65; IGHV3-7; IGHV3-57; IGHV3-52; IGHV4-30-2; IGHVII-28-1; IGHVIII-22-2; IGH; SLC20A1P1; IGHV3-25; IGHV3-63; IGHV3-30-2; IGHV3-54; IGHVII-20-1; IGHV1-14; IGHV3-16; IGHV4-34; IGHV3-30; IGHVII-26-2; IGHV3-42; IGHVIII-26-1; IGHV4-55; IGHVII-49-1; LOC102724977; SLC20A1P2; IGHVIII-16-1; IGHVII-43-1; IGHV3-33-2; RNA5SP389; IGHVIII-5-2; IGHVII-15-1; GOLGA4P1; IGHV2-70D; IGHVIII-47-1; IGHV3-6; IGHV3-11; IGHV3-37; See more...

Location information:

ID:: 49475920

variant

18.

nsv4385955

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Location information:

ID:: 49476688

variant

19.

nsv4376591

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Location information:

ID:: 49467324

variant

20.

nsv4368660

Variant type:: copy number variation

Associated study:: nstd173

Organism:
human

Location information:

ID:: 49459393

variant

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222684 AND nstd173 (26)
dbVar
Homo sapiens isolate CHM13 chromosome 12, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 12, alternate assembly T2T-CHM13v2.0
gi|2194973269|gnl|ASM:GCF_009914825 ef|NC_060936.1||gpp|GPC_000012751.1||gnl|NCBI_GENOMES|119572

Nucleotide
Taxonomy Links for Protein (Select 1209185320) (1)
Taxonomy
Genome Links for Protein (Select 2217372991) (1)
Genome
Homo sapiens
Homo sapiens

Genome

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