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Items: 1 to 20 of 135

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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
    nsv5900364copy number variation1nstd209human GRCh38 chr4: 22,726,483-22,726,544 , GRCh37.p13 chr4: 22,728,106-22,728,167 , GBA3, 1 more genes
    nsv5575586copy number variation1nstd207human GRCh38 chr4: 22,726,462-22,726,523 , GRCh37.p13 chr4: 22,728,085-22,728,146 , GBA3, 1 more genes
    nsv5563071sequence alteration1nstd206human GRCh38 chr4: 22,590,995-23,538,734 , GRCh37.p13 chr4: 22,592,618-23,540,357 , GBA3, 7 more genes
    nsv5448261copy number variation1nstd206human GRCh38 chr4: 22,724,768-22,726,362 , GRCh37.p13 chr4: 22,726,391-22,727,985 , GBA3, 1 more genes
    nsv5444229copy number variation1nstd206human GRCh38 chr4: 22,699,132-22,775,478 , GRCh37.p13 chr4: 22,700,755-22,777,101 , GBA3, 2 more genes
    nsv5435123copy number variation1nstd206human GRCh38 chr4: 22,720,662-22,726,593 , GRCh37.p13 chr4: 22,722,285-22,728,216 , CDC42P6, 1 more genes
    nsv5232139copy number variation1nstd204human GRCh37.p13 chr4: 22,592,324-23,172,523 , GRCh38.p13 chr4: 22,590,701-23,170,900 , GBA3, 5 more genes
    nsv5223238copy number variation1nstd204human GRCh38.p13 chr4: 22,711,175-22,749,375 , GRCh37.p13 chr4: 22,712,798-22,750,998 , CDC42P6, 2 more genes
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv4921921copy number variation1nstd200human GRCh38 chr4: 22,724,768-22,726,362 , GRCh37.p13 chr4: 22,726,391-22,727,985 , CDC42P6, 1 more genes
    nsv4921911copy number variation1nstd200human GRCh38 chr4: 22,638,659-23,188,661 , GRCh37.p13 chr4: 22,640,282-23,190,284 , GBA3, 4 more genes
    nsv4799738copy number variation1nstd200human GRCh37 chr4: 22,726,391-22,727,985 , GRCh38.p12 chr4: 22,724,768-22,726,362 , CDC42P6, 1 more genes
    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
    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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