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 112

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 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
    nsv5033844inversion1nstd200human GRCh38 chr4: 151,269,541-154,434,055 , GRCh37.p13 chr4: 152,190,693-155,355,207 RNU6-1282P, RNF175, 47 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
    nsv4674602copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 153,061,243-157,994,448 , GRCh38.p12 chr4: 152,140,091-157,073,296 ANXA2P1, CTSO, 84 more genes
    nsv4473706mobile element insertion1nstd166human GRCh37.p13 chr4: 154,228,288-154,228,288 , GRCh38.p12 chr4: 153,307,136-153,307,136 ANXA2P1, TRIM2
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
    nsv4379217copy number variation1nstd173human GRCh37 chr4: 153,432,884-155,038,832 , GRCh38.p12 chr4: 152,511,732-154,117,680 RPS3AP18, LOC105377496, 26 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
    nsv4103698copy number variation1nstd166human GRCh37.p13 chr4: 154,126,000-154,242,000 , GRCh38.p12 chr4: 153,204,848-153,320,848 RNU6-1196P, LOC105377496, 2 more genes
    nsv3966753copy number variation1nstd168human GRCh38 chr4: 153,306,393-153,373,748 , GRCh37.p13 chr4: 154,227,545-154,294,900 ANXA2P1, MND1, 1 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
    nsv3922745copy number variation1nstd102humanPathogenic NCBI36 chr4: 139,651,136-191,121,344 , GRCh37 chr4: 139,431,686-190,828,225 , GRCh38 chr4: 138,510,532-189,963,195 TMEM131L, MTCO1P9, 622 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
    nsv3916456copy number variation1nstd102humanPathogenic GRCh38 chr4: 145,042,668-189,975,519 , NCBI36 chr4: 146,183,270-191,133,668 , GRCh37 chr4: 145,963,820-190,828,225 LOC107986328, MARK2P4, 546 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