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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5532297copy number variation1nstd206human GRCh38 chr19: 10,311,420-10,312,649 , GRCh37.p13 chr19: 10,422,096-10,423,325 FDX2
    nsv5519969copy number variation1nstd206human GRCh38 chr19: 10,312,065-10,313,853 , GRCh37.p13 chr19: 10,422,741-10,424,529 FDX2
    nsv5288069copy number variation1nstd204human GRCh38.p13 chr19: 10,216,408-10,327,822 , GRCh37.p13 chr19: 10,327,084-10,438,498 FDX2, MRPL4, 9 more genes
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5011607copy number variation1nstd200human GRCh38 chr19: 10,311,493-10,312,767 , GRCh37.p13 chr19: 10,422,169-10,423,443 FDX2
    nsv4852983copy number variation1nstd200human GRCh37 chr19: 10,422,342-10,423,408 , GRCh38.p12 chr19: 10,311,666-10,312,732 FDX2
    nsv4671580copy number variation1nstd186human GRCh37 chr19: 10,421,989-10,423,134 , GRCh38.p12 chr19: 10,311,313-10,312,458 FDX2
    nsv4623821copy number variation1nstd183human GRCh37 chr19: 10,421,989-10,423,134 , GRCh38.p12 chr19: 10,311,313-10,312,458 FDX2
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 more genes
    nsv3920643copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688 MIR4748, ZGLP1, 36 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3900924copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,286,133-11,040,457 , GRCh38.p12 chr19: 10,175,457-10,929,781 MIR4322, QTRT1, 38 more genes
    nsv3898900copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614 FBXL12, DCAF15, 253 more genes
    nsv3167259copy number variation1nstd151human GRCh37 chr19: 10,259,557-10,946,034 , GRCh38.p12 chr19: 10,148,881-10,835,358 RAVER1, ILF3-DT, 35 more genes
    nsv3166981copy number variation1nstd151human GRCh37 chr19: 10,124,112-10,421,621 , GRCh38.p12 chr19: 10,013,436-10,310,945 ANGPTL6, EIF3G, 20 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