U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 132

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905834copy number variation1nstd209human GRCh38 chr4: 121,812,027-121,818,718 , GRCh37.p13 chr4: 122,733,182-122,739,873 EXOSC9, CCNA2
    nsv5837605copy number variation1nstd209human GRCh38 chr4: 121,811,994-121,818,450 , GRCh37.p13 chr4: 122,733,149-122,739,605 CCNA2, EXOSC9
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5457197copy number variation1nstd206human GRCh38 chr4: 121,812,027-121,818,723 , GRCh37.p13 chr4: 122,733,182-122,739,878 EXOSC9, CCNA2
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5377651translocation1nstd200human GRCh38 chr4: 121,812,027-121,812,027 , GRCh38 chr4: 121,818,722-121,818,722 , GRCh37.p13 chr4: 122,739,877-122,739,877 , GRCh37.p13 chr4: 122,733,182-122,733,182 CCNA2, EXOSC9
    nsv5308603copy number variation1nstd204human GRCh38.p13 chr4: 121,812,022-121,818,732 , GRCh37.p13 chr4: 122,733,177-122,739,887 CCNA2, EXOSC9
    nsv5237137copy number variation1nstd204human GRCh38.p13 chr4: 121,811,509-121,818,550 , GRCh37.p13 chr4: 122,732,664-122,739,705 CCNA2, EXOSC9
    nsv5235449copy number variation1nstd204human GRCh38.p13 chr4: 121,812,001-121,818,700 , GRCh37.p13 chr4: 122,733,156-122,739,855 CCNA2, EXOSC9
    nsv5227883copy number variation1nstd204human GRCh38.p13 chr4: 121,811,794-121,818,550 , GRCh37.p13 chr4: 122,732,949-122,739,705 EXOSC9, CCNA2
    nsv5222129copy number variation1nstd204human GRCh38.p13 chr4: 121,810,401-121,818,800 , GRCh37.p13 chr4: 122,731,556-122,739,955 CCNA2, EXOSC9
    nsv4794448copy number variation1nstd200human GRCh37 chr4: 122,733,182-122,739,878 , GRCh38.p12 chr4: 121,812,027-121,818,723 EXOSC9, CCNA2
    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
    nsv4455247copy number variation1nstd102humanUncertain significance GRCh37 chr4: 122,547,684-123,268,279 , GRCh38.p12 chr4: 121,626,529-122,347,124 ANXA5, LOC105377402, 10 more genes
    nsv4436254copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 116,624,547-126,168,646 , GRCh38.p12 chr4: 115,703,391-125,247,491 ANXA5, CCNA2, 125 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center