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 161

    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
    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
    nsv7064657inversion1nstd229human GRCh38 chr19: 40,789,467-40,797,201 , GRCh37.p13 chr19: 41,295,372-41,303,106 MIA-RAB4B, RAB4B-EGLN2, 2 more genes
    nsv7015974copy number variation1nstd229human GRCh38 chr19: 40,795,453-40,804,521 , GRCh37.p13 chr19: 41,301,358-41,310,426 RAB4B-EGLN2, RAB4B, 2 more genes
    nsv7014993copy number variation1nstd229human GRCh38 chr19: 40,791,269-40,795,675 , GRCh37.p13 chr19: 41,297,174-41,301,580 RAB4B, MIA-RAB4B, 1 more genes
    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
    nsv7002197copy number variation1nstd229human GRCh38 chr19: 40,791,836-40,795,557 , GRCh37.p13 chr19: 41,297,741-41,301,462 RAB4B-EGLN2, MIA-RAB4B, 1 more genes
    nsv6599698inversion1nstd223human GRCh38 chr19: 40,794,888-40,795,586 , GRCh37.p13 chr19: 41,300,793-41,301,491 RAB4B, MIA-RAB4B, 1 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6532674copy number variation1nstd223human GRCh38 chr19: 40,791,284-40,795,646 , GRCh37.p13 chr19: 41,297,189-41,301,551 RAB4B-EGLN2, RAB4B, 1 more genes
    nsv6527221copy number variation1nstd223human GRCh38 chr19: 40,790,624-40,791,241 , GRCh37.p13 chr19: 41,296,529-41,297,146 MIA-RAB4B, RAB4B-EGLN2, 1 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6144971copy number variation1nstd206human GRCh38 chr19: 40,708,874-40,776,874 , GRCh37.p13 chr19: 41,214,779-41,282,779 SNRPA, MIA, 6 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6048170copy number variation1nstd212human GRCh38 chr19: 40,770,782-40,781,743 , GRCh37.p13 chr19: 41,276,687-41,287,648 MIA, RAB4B, 2 more genes
    nsv5886816copy number variation1nstd209human GRCh38 chr19: 40,787,533-40,788,800 , GRCh37.p13 chr19: 41,293,438-41,294,705 RAB4B, MIA-RAB4B, 1 more genes
    nsv5525814copy number variation1nstd206human GRCh38 chr19: 40,786,080-40,786,320 , GRCh37.p13 chr19: 41,291,985-41,292,225 MIA-RAB4B, RAB4B-EGLN2, 1 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