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 156

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7077839inversion1nstd229human GRCh38 chr19: 41,720,382-41,720,426 , GRCh37.p13 chr19|NW_004775434.1: 289,421-289,465 , GRCh37.p13 chr19: 42,224,301-42,224,345 CEACAM5
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7061861inversion1nstd229human GRCh38 chr19: 41,686,845-41,727,624 , GRCh37.p13 chr19|NW_004775434.1: 255,884-296,663 , GRCh37.p13 chr19: 42,190,776-42,231,544 CEACAM5, CEACAM7
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv6998554copy number variation1nstd229human GRCh38 chr19: 41,717,027-41,717,254 , GRCh37.p13 chr19|NW_004775434.1: 286,066-286,293 , GRCh37.p13 chr19: 42,220,946-42,221,173 CEACAM5
    nsv6599527inversion1nstd223human GRCh38 chr19: 41,722,943-41,723,792 , GRCh37.p13 chr19: 42,226,863-42,227,712 , GRCh37.p13 chr19|NW_004775434.1: 291,982-292,831 CEACAM5
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6525620copy number variation1nstd223human GRCh38 chr19: 41,715,127-41,720,050 , GRCh37.p13 chr19: 42,219,046-42,223,969 , GRCh37.p13 chr19|NW_004775434.1: 284,166-289,089 CEACAM5
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv5298443copy number variation1nstd204human GRCh38.p13 chr19: 41,726,675-41,727,774 , GRCh37.p13 chr19: 42,230,595-42,231,694 , GRCh37.p13 chr19|NW_004775434.1: 295,714-296,813 CEACAM5
    nsv5293732copy number variation1nstd204human GRCh38.p13 chr19: 41,614,001-41,747,800 , GRCh37.p13 chr19|NW_004775434.1: 183,040-316,839 , GRCh37.p13 chr19: 42,120,357-42,251,720 LOC105372405, CEACAM5, 3 more genes
    nsv5024657copy number variation1nstd200human GRCh38 chr19: 41,714,885-41,720,026 , GRCh37.p13 chr19: 42,218,804-42,223,945 , GRCh37.p13 chr19|NW_004775434.1: 283,924-289,065 CEACAM5
    nsv5020496copy number variation1nstd200human GRCh38 chr19: 41,715,125-41,720,052 , GRCh37.p13 chr19|NW_004775434.1: 284,164-289,091 , GRCh37.p13 chr19: 42,219,044-42,223,971 CEACAM5
    nsv4868430copy number variation1nstd200human GRCh37 chr19: 42,219,044-42,223,971 , GRCh38.p12 chr19: 41,715,125-41,720,052 CEACAM5
    nsv4702641copy number variation1nstd195human GRCh37 chr19: 41,998,201-42,367,401 , GRCh38.p12 chr19: 41,492,293-41,863,329 , GRCh38.p12 chr19|NT_187620.1: 1-198,050 CEACAM5, CEACAM7, 20 more genes
    nsv4676231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,889,319-42,338,832 , GRCh38.p12 chr19: 41,383,414-41,834,777 , GRCh38.p12 chr19|NT_187620.1: 1-233,762 CEACAM7, LYPD4, 25 more genes
    nsv4533263copy number variation1nstd166human GRCh37.p13 chr19: 42,227,355-42,230,651 , GRCh38.p12 chr19: 41,723,435-41,726,731 CEACAM5
    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