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 119

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4934947copy number variation1nstd200human GRCh38 chr4: 101,348,052-101,351,772 , GRCh37.p13 chr4: 102,269,209-102,272,929 PPP3CA, FLJ20021
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 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
    nsv4396373copy number variation1nstd174human GRCh37 chr4: 102,266,545-102,269,492 , GRCh38.p12 chr4: 101,345,388-101,348,335 FLJ20021, PPP3CA
    nsv4371813copy number variation1nstd173human GRCh37 chr4: 102,236,321-102,283,898 , GRCh38.p12 chr4: 101,315,164-101,362,741 FLJ20021, PPP3CA, 1 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
    nsv4337628sequence alteration1nstd166human GRCh37.p13 chr4: 95,972,584-105,073,318 , GRCh38.p12 chr4: 95,051,433-104,152,161 , ADH1B, 98 more genes
    nsv4096491copy number variation1nstd166human GRCh37.p13 chr4: 102,246,492-102,357,005 , GRCh38.p12 chr4: 101,325,335-101,435,848 PPP3CA, FLJ20021, 1 more genes
    nsv3920440copy number variation1nstd102humanUncertain significance NCBI36 chr4: 101,719,190-102,662,230 , GRCh37 chr4: 101,500,167-102,443,207 , GRCh38 chr4: 100,579,010-101,522,050 FLJ20021, LINC01216, 4 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
    nsv3910689copy number variation1nstd102humanPathogenic GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171 GRID2, ABT1P1, 77 more genes
    nsv3885328copy number variation1nstd102humanPathogenic GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651 TRMT10A, TBCAP3, 86 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 MTND4LP29, RNU6-128P, 2341 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