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 954

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7144055copy number variation1nstd232human GRCh37.p13 chr4: 5,145,501-5,145,558 , GRCh38.p12 chr4: 5,143,774-5,143,831 STK32B
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7057453inversion1nstd229human GRCh38 chr4: 5,450,623-5,450,662 , GRCh37.p13 chr4: 5,452,350-5,452,389 STK32B
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 more genes
    nsv7054237inversion1nstd229human GRCh38 chr4: 5,484,109-5,520,788 , GRCh37.p13 chr4: 5,485,836-5,522,515 STK32B
    nsv7052787inversion1nstd229human GRCh38 chr4: 5,362,348-5,365,742 , GRCh37.p13 chr4: 5,364,075-5,367,469 STK32B
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7042504inversion1nstd229human GRCh38 chr4: 5,218,293-5,218,388 , GRCh37.p13 chr4: 5,220,020-5,220,115 STK32B
    nsv7041350inversion1nstd229human GRCh38 chr4: 5,397,017-5,397,078 , GRCh37.p13 chr4: 5,398,744-5,398,805 STK32B
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6738032copy number variation1nstd229human GRCh38 chr4: 5,289,701-5,295,500 , GRCh37.p13 chr4: 5,291,428-5,297,227 STK32B
    nsv6737636copy number variation1nstd229human GRCh38 chr4: 5,375,413-5,384,347 , GRCh37.p13 chr4: 5,377,140-5,386,074 STK32B
    nsv6737581copy number variation1nstd229human GRCh38 chr4: 5,248,111-5,248,267 , GRCh37.p13 chr4: 5,249,838-5,249,994 STK32B
    nsv6737480copy number variation1nstd229human GRCh38 chr4: 5,053,259-5,085,039 , GRCh37.p13 chr4: 5,054,986-5,086,766 STK32B
    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