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 469

    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
    nsv7095258copy number variation1nstd102humanUncertain significance GRCh37 chr18: 9,102,742-12,725,530 , GRCh38.p12 chr18: 9,102,744-12,725,531 PIEZO2, RALBP1, 77 more genes
    nsv7076310inversion1nstd229human GRCh38 chr18: 7,168,687-9,983,107 , GRCh37.p13 chr18: 7,168,686-9,983,104 MTCL1, LOC112577592, 40 more genes
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7059490inversion1nstd229human GRCh38 chr18: 9,947,220-9,947,261 , GRCh37.p13 chr18: 9,947,217-9,947,258 VAPA
    nsv7015128copy number variation1nstd229human GRCh38 chr18: 4,434,377-14,413,632 , GRCh37.p13 chr18: 4,434,377-14,413,631 RAB31, THEMIS3P, 167 more genes
    nsv7010430copy number variation1nstd229human GRCh38 chr18: 9,931,901-9,937,000 , GRCh37.p13 chr18: 9,931,898-9,936,997 VAPA
    nsv7005498copy number variation1nstd229human GRCh38 chr18: 9,942,639-9,946,640 , GRCh37.p13 chr18: 9,942,636-9,946,637 VAPA
    nsv7004518copy number variation1nstd229human GRCh38 chr18: 9,956,401-10,306,200 , GRCh37.p13 chr18: 9,956,398-10,306,197 LOC105371983, LOC105371984, 1 more genes
    nsv7003223copy number variation1nstd229human GRCh38 chr18: 9,804,909-10,534,004 , GRCh37.p13 chr18: 9,804,906-10,534,001 RNA5SP450, VAPA, 15 more genes
    nsv6998358copy number variation1nstd229human GRCh38 chr18: 9,911,965-9,912,017 , GRCh37.p13 chr18: 9,911,962-9,912,014 VAPA
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6527185copy number variation1nstd223human GRCh38 chr18: 9,954,435-9,954,909 , GRCh37.p13 chr18: 9,954,432-9,954,906 VAPA
    nsv6519797copy number variation1nstd223human GRCh38 chr18: 9,920,188-9,920,505 , GRCh37.p13 chr18: 9,920,185-9,920,502 VAPA
    nsv6517298copy number variation1nstd223human GRCh38 chr18: 9,933,014-9,934,971 , GRCh37.p13 chr18: 9,933,011-9,934,968 VAPA
    nsv6315541copy number variation1nstd102humanPathogenic GRCh37 chr18: 9,569,601-12,218,695 , GRCh38.p12 chr18: 9,569,603-12,218,696 LOC105371989, LOC100533852, 55 more genes
    nsv6315536copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-10,172,941 , GRCh38.p12 chr18: 136,226-10,172,944 DLGAP1-AS5, TWSG1, 150 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6315508copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-14,632,436 , GRCh38.p12 chr18: 136,226-14,632,437 IGLJCOR18, MYOM1, 247 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