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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5905983copy number variation1nstd209human GRCh38 chr4: 21,446,075-21,465,748 , GRCh37.p13 chr4: 21,447,698-21,467,371 KCNIP4, MIR7978
    nsv5839224copy number variation1nstd209human GRCh38 chr4: 21,446,036-21,465,547 , GRCh37.p13 chr4: 21,447,659-21,467,170 MIR7978, KCNIP4
    nsv5450541copy number variation1nstd206human GRCh38 chr4: 21,464,610-21,533,591 , GRCh37.p13 chr4: 21,466,233-21,535,214 MIR7978, KCNIP4
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4925362copy number variation1nstd200human GRCh38 chr4: 21,399,211-21,615,929 , GRCh37.p13 chr4: 21,400,834-21,617,552 MIR7978, KCNIP4, 1 more genes
    nsv4925360copy number variation1nstd200human GRCh38 chr4: 21,300,651-21,742,142 , GRCh37.p13 chr4: 21,302,274-21,743,765 , KCNIP4, 3 more genes
    nsv4925359copy number variation1nstd200human GRCh38 chr4: 21,266,815-21,477,729 , GRCh37.p13 chr4: 21,268,438-21,479,352 MIR7978, KCNIP4
    nsv4921873copy number variation1nstd200human GRCh38 chr4: 21,446,077-21,465,749 , GRCh37.p13 chr4: 21,447,700-21,467,372 KCNIP4, MIR7978
    nsv4809086copy number variation1nstd200human GRCh37 chr4: 21,400,834-21,617,553 , GRCh38.p12 chr4: 21,399,211-21,615,930 MIR7978, KCNIP4, 1 more genes
    nsv4809084copy number variation1nstd200human GRCh37 chr4: 21,302,274-21,743,765 , GRCh38.p12 chr4: 21,300,651-21,742,142 , MIR7978, 3 more genes
    nsv4799705copy number variation1nstd200human GRCh37 chr4: 21,447,700-21,467,372 , GRCh38.p12 chr4: 21,446,077-21,465,749 MIR7978, KCNIP4
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4679577copy number variation1nstd189human GRCh37.p13 chr4: 20,966,386-21,647,088 , GRCh38.p12 chr4: 20,964,763-21,645,465 KCNIP4, MIR7978, 1 more genes
    nsv4674448copy number variation1nstd102humanPathogenic GRCh37 chr4: 20,406,475-29,134,345 , GRCh38.p12 chr4: 20,404,852-29,132,723 LOC100288962, ADGRA3, 84 more genes
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