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 254

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095644copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,456,055-2,456,931 , GRCh38.p12 chr19: 1,456,056-2,456,933 APC2, CSNK1G2, 49 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 NDUFS7, GAMT, 30 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7070296inversion1nstd229human GRCh38 chr19: 1,461,618-2,158,584 , GRCh37.p13 chr19: 1,461,617-2,158,583 BTBD2, MEX3D, 30 more genes
    nsv7012224copy number variation1nstd229human GRCh38 chr19: 1,597,295-1,609,238 , GRCh37.p13 chr19: 1,597,294-1,609,237 TCF3, UQCR11
    nsv7006261copy number variation1nstd229human GRCh38 chr19: 1,420,401-1,679,000 , GRCh37.p13 chr19: 1,420,400-1,678,999 C19orf25, PLK5, 13 more genes
    nsv7005086copy number variation1nstd229human GRCh38 chr19: 1,581,329-1,609,252 , GRCh37.p13 chr19: 1,581,328-1,609,251 UQCR11, MBD3, 1 more genes
    nsv6637582copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,356,893-1,676,446 , GRCh38.p12 chr19: 1,356,894-1,676,447 REEP6, GAMT, 18 more genes
    nsv6533604copy number variation1nstd223human GRCh38 chr19: 1,595,739-1,596,644 , GRCh37.p13 chr19: 1,595,738-1,596,643 UQCR11
    nsv6527194copy number variation1nstd223human GRCh38 chr19: 1,600,895-1,601,329 , GRCh37.p13 chr19: 1,600,894-1,601,328 UQCR11
    nsv6520307copy number variation1nstd223human GRCh38 chr19: 1,596,506-1,598,281 , GRCh37.p13 chr19: 1,596,505-1,598,280 UQCR11
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6133707copy number variation1nstd213human GRCh37 chr19: 560,000-1,700,001 , GRCh38.p12 chr19: 560,000-1,700,002 ATP5F1D, AZU1, 73 more genes
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
    nsv6046460copy number variation1nstd212human GRCh38 chr19: 1,600,430-1,607,658 , GRCh37.p13 chr19: 1,600,429-1,607,657 UQCR11, TCF3
    nsv5935756copy number variation1nstd209human GRCh38 chr19: 1,600,495-1,608,281 , GRCh37.p13 chr19: 1,600,494-1,608,280 UQCR11, TCF3
    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