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 265

    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
    nsv7074186inversion1nstd229human GRCh38 chr18: 7,953,048-15,343,982 , GRCh37.p13 chr18: 7,953,046-15,343,981 PSMG2, EIF4A2P1, 155 more genes
    nsv7068129inversion1nstd229human GRCh38 chr18: 10,146,300-12,104,874 , GRCh37.p13 chr18: 10,146,297-12,104,873 LOC105371993, KIAA0895LP1, 35 more genes
    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
    nsv7013158copy number variation1nstd229human GRCh38 chr18: 10,379,249-10,533,409 , GRCh37.p13 chr18: 10,379,246-10,533,406 LOC105371989, LINC01254, 3 more genes
    nsv7006757copy number variation1nstd229human GRCh38 chr18: 10,031,532-10,442,585 , GRCh37.p13 chr18: 10,031,529-10,442,582 LOC105371984, LOC105371986, 4 more genes
    nsv7006677copy number variation1nstd229human GRCh38 chr18: 10,115,047-11,546,327 , GRCh37.p13 chr18: 10,115,044-11,546,326 PMM2P1, MIR6788, 19 more genes
    nsv7006202copy number variation1nstd229human GRCh38 chr18: 10,360,632-11,170,948 , GRCh37.p13 chr18: 10,360,629-11,170,947 LINC01887, LOC105371986, 12 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
    nsv7001813copy number variation1nstd229human GRCh38 chr18: 10,003,114-10,519,207 , GRCh37.p13 chr18: 10,003,111-10,519,204 LOC105371985, LOC105371988, 6 more genes
    nsv7001429copy number variation1nstd229human GRCh38 chr18: 10,406,550-10,408,769 , GRCh37.p13 chr18: 10,406,547-10,408,766 LINC01254, LOC105371988
    nsv6638027copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,344,636-11,185,412 , GRCh38.p12 chr18: 10,344,639-11,185,413 NAPG, KIAA0895LP1, 12 more genes
    nsv6637285copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-11,283,184 , GRCh38.p12 chr18: 136,227-11,283,185 EMILIN2, KRT18P8, 165 more genes
    nsv6533384copy number variation1nstd223human GRCh38 chr18: 10,379,249-10,533,407 , GRCh37.p13 chr18: 10,379,246-10,533,404 APCDD1, LINC01254, 3 more genes
    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
    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
    nsv6315187copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,390-14,854,037 , GRCh38.p12 chr18: 47,390-14,854,038 MIR4526, LINC01882, 261 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