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 111

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4943853copy number variation1nstd200human GRCh38 chr4: 112,771,372-112,799,085 , GRCh37.p13 chr4: 113,692,528-113,720,241 LOC100131158, ANK2, 1 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4794405copy number variation1nstd200human GRCh37 chr4: 113,692,528-113,720,241 , GRCh38.p12 chr4: 112,771,372-112,799,085 LOC100131158, ANK2, 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
    nsv4374635copy number variation1nstd173human GRCh37 chr4: 111,109,020-113,950,046 , GRCh38.p12 chr4: 110,187,864-113,028,890 , HSBP1P2, 52 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4328272inversion1nstd166human GRCh37.p13 chr4: 110,343,023-114,944,660 , GRCh38.p12 chr4: 109,421,867-114,023,504 , EGF, 82 more genes
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 MIR576, ABT1P1, 447 more genes
    nsv3916833copy number variation1nstd102humanUncertain significance NCBI36 chr4: 113,595,184-114,437,140 , GRCh37.p13 chr4: 113,375,735-114,217,691 , GRCh38.p12 chr4: 112,454,579-113,296,535 MIR302CHG, MIR302A, 23 more genes
    nsv3916316copy number variation1nstd102humanUncertain significance NCBI36 chr4: 111,318,515-191,263,063 , GRCh37.p13 chr4: 111,099,066-191,029,082 , GRCh38.p12 chr4: 110,177,910-190,107,927 RNU7-194P, FOSL1P1, 939 more genes
    nsv3914452copy number variation1nstd102humanUncertain significance GRCh37 chr4: 113,610,380-114,357,626 , GRCh38 chr4: 112,689,224-113,436,470 , NCBI36 chr4: 113,829,829-114,577,075 RN7SL184P, RPS26P25, 12 more genes
    nsv3912675copy number variation1nstd102humanUncertain significance GRCh37 chr4: 113,485,538-113,744,392 , NCBI36 chr4: 113,704,987-113,963,841 , GRCh38 chr4: 112,564,382-112,823,236 ANK2, RPL32P13, 13 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center