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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047284inversion1nstd229human GRCh38 chr5: 18,365,039-24,500,882 , GRCh37.p13 chr5: 18,365,148-24,500,991 LOC105374683, SNORA105A, 40 more genes
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7046828inversion1nstd229human GRCh38 chr5: 18,870,000-23,244,369 , GRCh37.p13 chr5: 18,870,109-23,244,478 LOC105374683, GUSBP1, 28 more genes
    nsv7045172inversion1nstd229human GRCh38 chr5: 18,376,939-24,500,874 , GRCh37.p13 chr5: 18,377,048-24,500,983 LOC102723561, LOC100420804, 40 more genes
    nsv7041231inversion1nstd229human GRCh38 chr5: 19,417,693-22,066,972 , GRCh37.p13 chr5: 19,417,802-22,067,081 LOC102723561, HSPD1P1, 16 more genes
    nsv6777396copy number variation1nstd229human GRCh38 chr5: 21,849,550-21,989,615 , GRCh37.p13 chr5: 21,849,659-21,989,724 CDH12, SNORA105A, 2 more genes
    nsv6777395copy number variation1nstd229human GRCh38 chr5: 21,698,901-23,136,400 , GRCh37.p13 chr5: 21,699,010-23,136,509 GCNT1P2, LOC101929617, 9 more genes
    nsv6772568copy number variation1nstd229human GRCh38 chr5: 21,874,932-21,897,579 , GRCh37.p13 chr5: 21,875,041-21,897,688 HSPD1P1, CDH12, 1 more genes
    nsv6765832copy number variation1nstd229human GRCh38 chr5: 21,643,360-22,014,178 , GRCh37.p13 chr5: 21,643,469-22,014,287 SNORA105A, LOC107986345, 4 more genes
    nsv6759139copy number variation1nstd229human GRCh38 chr5: 18,173,837-22,856,339 , GRCh37.p13 chr5: 18,173,946-22,856,448 CDH12, LOC105374685, 28 more genes
    nsv6758719copy number variation1nstd229human GRCh38 chr5: 18,040,306-26,567,940 , GRCh37.p13 chr5: 18,040,415-26,568,049 CDH12, LINC02899, 49 more genes
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636843copy number variation1nstd102humanUncertain significance GRCh37 chr5: 21,633,198-22,012,296 , GRCh38.p12 chr5: 21,633,089-22,012,187 LOC107986345, HSPD1P1, 4 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6630589copy number variation1nstd224human GRCh37 chr5: 21,585,236-21,917,519 , GRCh38.p12 chr5: 21,585,127-21,917,410 CDH12, HSPD1P1, 4 more genes
    nsv6630514copy number variation1nstd224human GRCh37 chr5: 18,548,150-22,081,601 , GRCh38.p12 chr5: 18,548,041-22,081,492 NUP50P3, LOC100419319, 23 more genes
    nsv6630332copy number variation1nstd224human GRCh37 chr5: 21,854,775-21,961,088 , GRCh38.p12 chr5: 21,854,666-21,960,979 HSPD1P1, CDH12, 1 more genes
    nsv6630331copy number variation1nstd224human GRCh37 chr5: 21,847,419-21,961,088 , GRCh38.p12 chr5: 21,847,310-21,960,979 HSPD1P1, SNORA105A, 1 more genes
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