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 165

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7076311inversion1nstd229human GRCh38 chr8: 100,143,600-100,150,543 , GRCh37.p13 chr8: 101,155,828-101,162,771 POLR2K, FBXO43
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv6858022copy number variation1nstd229human GRCh38 chr8: 100,093,901-100,262,000 , GRCh37.p13 chr8: 101,106,129-101,274,228 UFM1P3, RNF19A, 5 more genes
    nsv6847395copy number variation1nstd229human GRCh38 chr8: 100,007,701-100,261,900 , GRCh37.p13 chr8: 101,019,929-101,274,128 UFM1P3, RNF19A, 5 more genes
    nsv6844195copy number variation1nstd229human GRCh38 chr8: 100,151,601-100,163,600 , GRCh37.p13 chr8: 101,163,829-101,175,828 POLR2K, SPAG1, 1 more genes
    nsv6637993copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,384-101,278,033 , GRCh38.p12 chr8: 99,779,156-100,265,805 RNF19A, POLR2K, 8 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6431923copy number variation1nstd223human GRCh38 chr8: 100,135,501-100,173,600 , GRCh37.p13 chr8: 101,147,729-101,185,828 UFM1P3, SPAG1, 2 more genes
    nsv6431866copy number variation1nstd223human GRCh38 chr8: 100,094,901-100,165,200 , GRCh37.p13 chr8: 101,107,129-101,177,428 UFM1P3, SPAG1, 3 more genes
    nsv6422365copy number variation1nstd223human GRCh38 chr8: 100,146,601-100,150,500 , GRCh37.p13 chr8: 101,158,829-101,162,728 FBXO43, POLR2K
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6312665copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,135,566-106,815,766 , GRCh38.p12 chr8: 98,123,338-105,803,538 RNU6-748P, RN7SKP85, 144 more genes
    nsv6137320copy number variation1nstd213human GRCh37 chr8: 96,440,000-102,500,001 , GRCh38.p12 chr8: 95,427,772-101,487,773 SDC2, RGS22, 102 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135804copy number variation1nstd213human GRCh37 chr8: 101,120,000-101,190,001 , GRCh38.p12 chr8: 100,107,772-100,177,773 POLR2K, SPAG1, 2 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