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 111

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095477copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,927,663-19,312,528 , GRCh38.p12 chr19: 17,816,854-19,201,719 BORCS8, ARMC6, 60 more genes
    nsv7095199copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,304,756-19,304,962 , GRCh38.p12 chr19: 19,193,947-19,194,153 RFXANK
    nsv7076266inversion1nstd229human GRCh38 chr19: 19,130,894-20,543,167 , GRCh37.p13 chr19: 19,241,703-20,193,556 ZNF101, GATAD2A, 65 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7012541copy number variation1nstd229human GRCh38 chr19: 18,752,929-19,394,687 , GRCh37.p13 chr19: 18,863,739-19,505,496 SLC25A42, NCAN, 24 more genes
    nsv7010752copy number variation1nstd229human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 more genes
    nsv7003698copy number variation1nstd229human GRCh38 chr19: 19,187,788-19,191,847 , GRCh37.p13 chr19: 19,298,597-19,302,656 BORCS8-MEF2B, RFXANK, 1 more genes
    nsv6998304copy number variation1nstd229human GRCh38 chr19: 19,184,157-19,193,662 , GRCh37.p13 chr19: 19,294,966-19,304,471 BORCS8-MEF2B, BORCS8, 1 more genes
    nsv6637313copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,218,464-19,494,045 , GRCh38.p12 chr19: 19,107,655-19,383,236 BORCS8-MEF2B, MAU2, 11 more genes
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6526873copy number variation1nstd223human GRCh38 chr19: 19,194,488-19,195,994 , GRCh37.p13 chr19: 19,305,297-19,306,803 RFXANK
    nsv6310474copy number variation1nstd102humanUncertain significance GRCh37 chr19: 18,893,725-19,312,528 , GRCh38.p12 chr19: 18,782,915-19,201,719 MEF2B, SLC25A42, 16 more genes
    nsv6310292copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,312,438-19,312,528 , GRCh38.p12 chr19: 19,201,629-19,201,719 RFXANK, NR2C2AP
    nsv6133402copy number variation1nstd213human GRCh37 chr19: 19,150,000-24,140,001 , GRCh38.p12 chr19: 19,039,191-23,957,199 , NCAN, 199 more genes
    nsv6133401copy number variation1nstd213human GRCh37 chr19: 19,110,000-24,140,001 , GRCh38.p12 chr19: 18,999,191-23,957,199 , NCAN, 200 more genes
    nsv6133400copy number variation1nstd213human GRCh37 chr19: 18,720,000-20,740,001 , GRCh38.p12 chr19: 18,609,190-20,557,195 COMP, NCAN, 81 more genes
    nsv6102553inversion1nstd212human GRCh38 chr19: 18,724,785-21,720,303 , GRCh37.p13 chr19: 18,835,595-21,903,105 , COMP, 127 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 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