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Items: 1 to 20 of 269

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    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
    nsv7097886copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,412,639-106,815,766 , GRCh38.p12 chr8: 103,400,411-105,803,538 LOC105375692, LOC105375696, 28 more genes
    nsv7077334inversion1nstd229human GRCh38 chr8: 102,796,562-104,427,483 , GRCh37.p13 chr8: 103,808,790-105,439,711 DCSTAMP, LOC107984007, 33 more genes
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7072980inversion1nstd229human GRCh38 chr8: 102,790,775-104,428,155 , GRCh37.p13 chr8: 103,803,003-105,440,383 DCSTAMP, ATP6V1C1, 33 more genes
    nsv7071951inversion1nstd229human GRCh38 chr8: 103,396,728-104,467,028 , GRCh37.p13 chr8: 104,408,956-105,479,256 PTMAP15, DPYS, 14 more genes
    nsv7071528inversion1nstd229human GRCh38 chr8: 103,103,016-104,690,333 , GRCh37.p13 chr8: 104,115,244-105,702,561 LOC105375690, DCAF13, 27 more genes
    nsv7064953inversion1nstd229human GRCh38 chr8: 103,384,252-103,415,354 , GRCh37.p13 chr8: 104,396,480-104,427,582 SLC25A32, DCAF13, 1 more genes
    nsv6856867copy number variation1nstd229human GRCh38 chr8: 103,290,214-103,958,039 , GRCh37.p13 chr8: 104,302,442-104,970,267 SNORD173, FZD6, 12 more genes
    nsv6856659copy number variation1nstd229human GRCh38 chr8: 103,431,470-103,530,373 , GRCh37.p13 chr8: 104,443,698-104,542,601 DCAF13, LOC105375690, 1 more genes
    nsv6855645copy number variation1nstd229human GRCh38 chr8: 103,436,380-103,461,070 , GRCh37.p13 chr8: 104,448,608-104,473,298 DCAF13
    nsv6854554copy number variation1nstd229human GRCh38 chr8: 103,419,952-103,425,398 , GRCh37.p13 chr8: 104,432,180-104,437,626 DCAF13
    nsv6854024copy number variation1nstd229human GRCh38 chr8: 103,436,427-103,447,697 , GRCh37.p13 chr8: 104,448,655-104,459,925 DCAF13
    nsv6853729copy number variation1nstd229human GRCh38 chr8: 103,390,201-103,415,400 , GRCh37.p13 chr8: 104,402,429-104,427,628 DCAF13, SLC25A32
    nsv6851891copy number variation1nstd229human GRCh38 chr8: 103,354,601-103,427,300 , GRCh37.p13 chr8: 104,366,829-104,439,528 DCAF13, CTHRC1, 2 more genes
    nsv6851852copy number variation1nstd229human GRCh38 chr8: 103,417,701-103,433,000 , GRCh37.p13 chr8: 104,429,929-104,445,228 DCAF13
    nsv6843518copy number variation1nstd229human GRCh38 chr8: 103,349,875-103,866,372 , GRCh37.p13 chr8: 104,362,103-104,878,600 PTMAP15, TARBP2P1, 8 more genes
    nsv6637517copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,370,102-104,770,147 , GRCh38.p12 chr8: 103,357,874-103,757,919 SLC25A32, LOC101101841, 7 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
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