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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055296inversion1nstd229human GRCh38 chr5: 23,417,472-23,625,373 , GRCh37.p13 chr5: 23,417,581-23,625,482 PRDM9
    nsv7053321inversion1nstd229human GRCh38 chr5: 23,205,487-23,975,843 , GRCh37.p13 chr5: 23,205,596-23,975,952 PTPN11P4, LINC02899, 4 more genes
    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
    nsv7045313inversion1nstd229human GRCh38 chr5: 23,409,558-23,625,585 , GRCh37.p13 chr5: 23,409,667-23,625,694 PRDM9
    nsv7045172inversion1nstd229human GRCh38 chr5: 18,376,939-24,500,874 , GRCh37.p13 chr5: 18,377,048-24,500,983 LOC102723561, LOC100420804, 40 more genes
    nsv6777405copy number variation1nstd229human GRCh38 chr5: 23,521,849-23,524,274 , GRCh37.p13 chr5: 23,521,958-23,524,383 PRDM9
    nsv6775129copy number variation1nstd229human GRCh38 chr5: 23,401,578-23,686,651 , GRCh37.p13 chr5: 23,401,687-23,686,760 PRDM9
    nsv6774829copy number variation1nstd229human GRCh38 chr5: 23,490,671-23,519,645 , GRCh37.p13 chr5: 23,490,780-23,519,754 PRDM9
    nsv6772165copy number variation1nstd229human GRCh38 chr5: 23,506,468-23,518,727 , GRCh37.p13 chr5: 23,506,577-23,518,836 PRDM9
    nsv6772034copy number variation1nstd229human GRCh38 chr5: 23,510,609-23,514,694 , GRCh37.p13 chr5: 23,510,718-23,514,803 PRDM9
    nsv6771943copy number variation1nstd229human GRCh38 chr5: 22,899,081-23,706,263 , GRCh37.p13 chr5: 22,899,190-23,706,372 PRDM9, LOC105374686, 4 more genes
    nsv6771142copy number variation1nstd229human GRCh38 chr5: 23,519,505-23,521,885 , GRCh37.p13 chr5: 23,519,614-23,521,994 PRDM9
    nsv6765253copy number variation1nstd229human GRCh38 chr5: 23,487,314-23,573,797 , GRCh37.p13 chr5: 23,487,423-23,573,906 PRDM9
    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
    nsv6758357copy number variation1nstd229human GRCh38 chr5: 23,494,466-23,557,970 , GRCh37.p13 chr5: 23,494,575-23,558,079 PRDM9
    nsv6758102copy number variation1nstd229human GRCh38 chr5: 22,276,907-24,693,876 , GRCh37.p13 chr5: 22,277,016-24,693,985 LINC02899, LOC105374686, 14 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 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
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