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 746

    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
    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
    nsv7055699inversion1nstd229human GRCh38 chr4: 7,177,879-7,980,235 , GRCh37.p13 chr4: 7,179,606-7,981,962 LOC105374371, SORCS2, 8 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
    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
    nsv6737444copy number variation1nstd229human GRCh38 chr4: 8,021,365-8,027,209 , GRCh37.p13 chr4: 8,023,092-8,028,936 ABLIM2
    nsv6737322copy number variation1nstd229human GRCh38 chr4: 7,992,298-8,005,047 , GRCh37.p13 chr4: 7,994,025-8,006,774 ABLIM2, MIR95
    nsv6736723copy number variation1nstd229human GRCh38 chr4: 7,969,037-7,973,342 , GRCh37.p13 chr4: 7,970,764-7,975,069 ABLIM2
    nsv6736313copy number variation1nstd229human GRCh38 chr4: 7,969,001-7,972,300 , GRCh37.p13 chr4: 7,970,728-7,974,027 ABLIM2
    nsv6735189copy number variation1nstd229human GRCh38 chr4: 8,071,057-8,326,595 , GRCh37.p13 chr4: 8,072,784-8,328,322 LINC02517, SH3TC1, 4 more genes
    nsv6732778copy number variation1nstd229human GRCh38 chr4: 8,116,240-8,123,781 , GRCh37.p13 chr4: 8,117,967-8,125,508 ABLIM2
    nsv6731511copy number variation1nstd229human GRCh38 chr4: 7,968,565-7,973,261 , GRCh37.p13 chr4: 7,970,292-7,974,988 ABLIM2
    nsv6729556copy number variation1nstd229human GRCh38 chr4: 8,104,628-8,149,382 , GRCh37.p13 chr4: 8,106,355-8,151,109 ABLIM2
    nsv6729123copy number variation1nstd229human GRCh38 chr4: 8,074,124-8,176,433 , GRCh37.p13 chr4: 8,075,851-8,178,160 GMPSP1, ABLIM2
    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