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 129

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964107insertion1nstd209human GRCh38 chr4: 122,448,202-122,448,202 , GRCh37.p13 chr4: 123,369,357-123,369,357 IL2
    nsv5681731mobile element insertion1nstd211human GRCh38 chr4: 122,448,737-122,448,737 , GRCh37.p13 chr4: 123,369,892-123,369,892 IL2
    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
    nsv5469907copy number variation1nstd206human GRCh38 chr4: 122,449,067-122,449,169 , GRCh37.p13 chr4: 123,370,222-123,370,324 IL2
    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
    nsv5180040mobile element insertion1nstd203human GRCh38 chr4: 122,454,357-122,454,374 , GRCh37.p13 chr4: 123,375,512-123,375,529 IL2
    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
    nsv4596833copy number variation1nstd183human GRCh37 chr4: 123,277,961-123,378,083 , GRCh38.p12 chr4: 122,356,806-122,456,928 IL2, BLTP1, 1 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
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4092695copy number variation1nstd166human GRCh37.p13 chr4: 122,666,831-123,632,075 , GRCh38.p12 chr4: 121,745,676-122,710,920 EXOSC9, TRPC3, 13 more genes
    nsv3924008copy number variation1nstd102humanPathogenic GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788 PPID, METTL14-DT, 828 more genes
    nsv3922957copy number variation1nstd102humanPathogenic GRCh37 chr4: 118,273,037-134,486,822 , GRCh38 chr4: 117,351,881-133,565,667 , NCBI36 chr4: 118,492,485-134,706,272 LOC102724158, LOC105377411, 168 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
    nsv3918110copy number variation1nstd102humanPathogenic NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225 SCRG1, KRT18P51, 770 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