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 76

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7016629copy number variation1nstd229human GRCh38 chr19: 49,308,301-49,310,900 , GRCh37.p13 chr19: 49,811,558-49,814,157 SLC6A16, MIR4324
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6524442copy number variation1nstd223human GRCh38 chr19: 49,288,581-49,317,631 , GRCh37.p13 chr19: 49,791,838-49,820,888 SLC6A16, MIR4324
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6251094mobile element insertion1nstd215human GRCh38 chr19: 49,307,724-49,307,724 , GRCh37.p13 chr19: 49,810,981-49,810,981 SLC6A16, MIR4324
    nsv6133706copy number variation1nstd213human GRCh37 chr19: 49,520,000-50,090,001 , GRCh38.p12 chr19: 49,016,743-49,586,744 CD37, CGB3, 51 more genes
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6050964copy number variation1nstd212human GRCh38 chr19: 49,304,508-49,307,044 , GRCh37.p13 chr19: 49,807,765-49,810,301 SLC6A16, MIR4324
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5020982copy number variation1nstd200human GRCh38 chr19: 49,308,376-49,309,394 , GRCh37.p13 chr19: 49,811,633-49,812,651 SLC6A16, MIR4324
    nsv5020980copy number variation1nstd200human GRCh38 chr19: 49,288,557-49,317,617 , GRCh37.p13 chr19: 49,791,814-49,820,874 MIR4324, SLC6A16
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4620353copy number variation1nstd183human GRCh37 chr19: 49,812,389-49,813,853 , GRCh38.p12 chr19: 49,309,132-49,310,596 SLC6A16, MIR4324
    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