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 719

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7075587inversion1nstd229human GRCh38 chr18: 499,678-1,806,279 , GRCh37.p13 chr18: 499,678-1,806,280 LOC105371954, COLEC12, 23 more genes
    nsv7070144inversion1nstd229human GRCh38 chr18: 599,101-1,058,089 , GRCh37.p13 chr18: 599,101-1,058,090 LOC105371952, TYMSOS, 10 more genes
    nsv7069227inversion1nstd229human GRCh38 chr18: 305,918-1,971,959 , GRCh37.p13 chr18: 305,918-1,971,960 LOC105371960, CLUL1, 26 more genes
    nsv7068154inversion1nstd229human GRCh38 chr18: 801,310-801,369 , GRCh37.p13 chr18: 801,311-801,370 YES1
    nsv7067968inversion1nstd229human GRCh38 chr18: 526,216-722,843 , GRCh37.p13 chr18: 526,216-722,843 CETN1, TYMS, 6 more genes
    nsv7064783inversion1nstd229human GRCh38 chr18: 632,722-843,391 , GRCh37.p13 chr18: 632,722-843,392 TYMSOS, RNU1-109P, 6 more genes
    nsv7062830inversion1nstd229human GRCh38 chr18: 594,354-744,826 , GRCh37.p13 chr18: 594,354-744,826 CLUL1, LOC105371952, 4 more genes
    nsv7060797inversion1nstd229human GRCh38 chr18: 563,827-764,945 , GRCh37.p13 chr18: 563,827-764,946 LOC105371952, CETN1, 6 more genes
    nsv7060170inversion1nstd229human GRCh38 chr18: 561,284-859,571 , GRCh37.p13 chr18: 561,284-859,572 TYMSOS, YES1, 9 more genes
    nsv7059777inversion1nstd229human GRCh38 chr18: 712,529-1,045,946 , GRCh37.p13 chr18: 712,529-1,045,947 ENOSF1, BOLA2P1, 6 more genes
    nsv7059342inversion1nstd229human GRCh38 chr18: 457,327-1,560,638 , GRCh37.p13 chr18: 457,327-1,560,639 RNU1-109P, CETN1, 22 more genes
    nsv6997814copy number variation1nstd229human GRCh38 chr18: 721,546-723,559 , GRCh37.p13 chr18: 721,546-723,559 YES1
    nsv6997807copy number variation1nstd229human GRCh38 chr18: 744,700-750,668 , GRCh37.p13 chr18: 744,700-750,668 YES1
    nsv6997693copy number variation1nstd229human GRCh38 chr18: 802,120-811,520 , GRCh37.p13 chr18: 802,121-811,521 YES1
    nsv6997233copy number variation1nstd229human GRCh38 chr18: 483,199-725,638 , GRCh37.p13 chr18: 483,199-725,638 ENOSF1, LINC01925, 8 more genes
    nsv6997196copy number variation1nstd229human GRCh38 chr18: 760,294-770,543 , GRCh37.p13 chr18: 760,294-770,544 YES1
    nsv6996744copy number variation1nstd229human GRCh38 chr18: 565,501-1,482,500 , GRCh37.p13 chr18: 565,501-1,482,501 LOC441806, LOC105371953, 19 more genes
    nsv6995190copy number variation1nstd229human GRCh38 chr18: 769,006-772,484 , GRCh37.p13 chr18: 769,007-772,485 YES1
    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