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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7076680inversion1nstd229human GRCh38 chr11: 72,466,691-73,774,399 , GRCh37.p13 chr11: 72,177,735-73,485,444 OR8R1P, PDE2A, 33 more genes
    nsv7075390inversion1nstd229human GRCh38 chr11: 72,466,687-73,774,399 , GRCh37.p13 chr11: 72,177,731-73,485,444 RAB6A, MIR139, 33 more genes
    nsv7061031inversion1nstd229human GRCh38 chr11: 73,050,314-73,050,351 , GRCh37.p13 chr11: 72,761,359-72,761,396 FCHSD2
    nsv7060486inversion1nstd229human GRCh38 chr11: 72,666,883-72,917,571 , GRCh37.p13 chr11: 72,377,927-72,628,616 PDE2A, FCHSD2, 9 more genes
    nsv6915754copy number variation1nstd229human GRCh38 chr11: 73,017,231-73,017,366 , GRCh37.p13 chr11: 72,728,276-72,728,411 FCHSD2
    nsv6915444copy number variation1nstd229human GRCh38 chr11: 73,048,103-73,052,513 , GRCh37.p13 chr11: 72,759,148-72,763,558 FCHSD2
    nsv6915044copy number variation1nstd229human GRCh38 chr11: 73,028,101-73,031,600 , GRCh37.p13 chr11: 72,739,146-72,742,645 FCHSD2
    nsv6914542copy number variation1nstd229human GRCh38 chr11: 73,036,970-73,037,090 , GRCh37.p13 chr11: 72,748,015-72,748,135 FCHSD2
    nsv6914388copy number variation1nstd229human GRCh38 chr11: 73,073,055-73,078,817 , GRCh37.p13 chr11: 72,784,100-72,789,862 FCHSD2
    nsv6914217copy number variation1nstd229human GRCh38 chr11: 72,925,849-72,931,880 , GRCh37.p13 chr11: 72,636,894-72,642,925 FCHSD2
    nsv6913704copy number variation1nstd229human GRCh38 chr11: 72,948,137-72,948,272 , GRCh37.p13 chr11: 72,659,182-72,659,317 FCHSD2
    nsv6912653copy number variation1nstd229human GRCh38 chr11: 72,876,403-72,876,929 , GRCh37.p13 chr11: 72,587,448-72,587,974 FCHSD2
    nsv6910011copy number variation1nstd229human GRCh38 chr11: 72,952,939-72,956,751 , GRCh37.p13 chr11: 72,663,984-72,667,796 FCHSD2
    nsv6909225copy number variation1nstd229human GRCh38 chr11: 72,852,852-72,854,910 , GRCh37.p13 chr11: 72,563,897-72,565,955 FCHSD2
    nsv6907955copy number variation1nstd229human GRCh38 chr11: 72,932,364-72,956,904 , GRCh37.p13 chr11: 72,643,409-72,667,949 RPL15P16, FCHSD2
    nsv6907774copy number variation1nstd229human GRCh38 chr11: 72,963,853-72,963,885 , GRCh37.p13 chr11: 72,674,898-72,674,930 FCHSD2
    nsv6907749copy number variation1nstd229human GRCh38 chr11: 73,028,119-73,031,643 , GRCh37.p13 chr11: 72,739,164-72,742,688 FCHSD2
    nsv6907724copy number variation1nstd229human GRCh38 chr11: 72,985,729-72,985,858 , GRCh37.p13 chr11: 72,696,774-72,696,903 FCHSD2
    nsv6906089copy number variation1nstd229human GRCh38 chr11: 72,989,036-72,989,478 , GRCh37.p13 chr11: 72,700,081-72,700,523 FCHSD2
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