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 489

    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
    nsv7142514insertion1nstd232human GRCh37.p13 chr4: 5,858,680-5,858,680 , GRCh38.p12 chr4: 5,856,953-5,856,953 CRMP1
    nsv7141664insertion1nstd232human GRCh37.p13 chr4: 5,858,712-5,858,712 , GRCh38.p12 chr4: 5,856,985-5,856,985 CRMP1
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    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
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7048274inversion1nstd229human GRCh38 chr4: 5,816,504-5,819,217 , GRCh37.p13 chr4: 5,818,231-5,820,944 CRMP1, EVC
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    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
    nsv6736739copy number variation1nstd229human GRCh38 chr4: 5,864,269-5,864,323 , GRCh37.p13 chr4: 5,865,996-5,866,050 CRMP1
    nsv6735000copy number variation1nstd229human GRCh38 chr4: 5,825,867-5,825,896 , GRCh37.p13 chr4: 5,827,594-5,827,623 EVC, CRMP1
    nsv6728852copy number variation1nstd229human GRCh38 chr4: 5,893,301-5,897,200 , GRCh37.p13 chr4: 5,895,028-5,898,927 C4orf50, CRMP1
    nsv6723709copy number variation1nstd229human GRCh38 chr4: 5,862,257-5,862,344 , GRCh37.p13 chr4: 5,863,984-5,864,071 CRMP1
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
    nsv6722593copy number variation1nstd229human GRCh38 chr4: 5,839,581-5,839,984 , GRCh37.p13 chr4: 5,841,308-5,841,711 CRMP1
    nsv6720883copy number variation1nstd229human GRCh38 chr4: 5,826,314-5,826,426 , GRCh37.p13 chr4: 5,828,041-5,828,153 CRMP1, EVC
    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