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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142233copy number variation1nstd232human GRCh37.p13 chr12: 95,387,007-95,387,142 , GRCh38.p12 chr12: 94,993,231-94,993,366 NDUFA12
    nsv7094060copy number variation1nstd102humanUncertain significance GRCh37 chr12: 95,396,495-95,397,456 , GRCh38.p12 chr12: 95,002,719-95,003,680 NDUFA12
    nsv7070416inversion1nstd229human GRCh38 chr12: 95,000,480-95,000,500 , GRCh37.p13 chr12: 95,394,256-95,394,276 NDUFA12
    nsv7065284inversion1nstd229human GRCh38 chr12: 94,129,761-97,319,471 , GRCh37.p13 chr12: 94,523,537-97,713,249 AMDHD1, TMCC3, 62 more genes
    nsv6937670copy number variation1nstd229human GRCh38 chr12: 94,999,215-94,999,722 , GRCh37.p13 chr12: 95,392,991-95,393,498 NDUFA12
    nsv6936355copy number variation1nstd229human GRCh38 chr12: 94,983,167-94,990,335 , GRCh37.p13 chr12: 95,376,943-95,384,111 NDUFA12
    nsv6935368copy number variation1nstd229human GRCh38 chr12: 94,982,601-94,985,200 , GRCh37.p13 chr12: 95,376,377-95,378,976 NDUFA12
    nsv6933448copy number variation1nstd229human GRCh38 chr12: 94,947,955-94,982,490 , GRCh37.p13 chr12: 95,341,731-95,376,266 NDUFA12
    nsv6928880copy number variation1nstd229human GRCh38 chr12: 95,001,999-95,017,062 , GRCh37.p13 chr12: 95,395,775-95,410,838 NDUFA12
    nsv6927794copy number variation1nstd229human GRCh38 chr12: 94,895,518-95,127,063 , GRCh37.p13 chr12: 95,289,294-95,520,839 NDUFA12, LOC105369915, 4 more genes
    nsv6927124copy number variation1nstd229human GRCh38 chr12: 94,982,560-94,985,352 , GRCh37.p13 chr12: 95,376,336-95,379,128 NDUFA12
    nsv6587635inversion1nstd223human GRCh38 chr12: 95,001,583-95,001,741 , GRCh37.p13 chr12: 95,395,359-95,395,517 NDUFA12
    nsv6470895copy number variation1nstd223human GRCh38 chr12: 94,982,559-94,985,351 , GRCh37.p13 chr12: 95,376,335-95,379,127 NDUFA12
    nsv6469678copy number variation1nstd223human GRCh38 chr12: 95,001,999-95,017,061 , GRCh37.p13 chr12: 95,395,775-95,410,837 NDUFA12
    nsv6274999copy number variation1nstd214human GRCh38 chr12: 94,985,491-94,985,549 , GRCh37.p13 chr12: 95,379,267-95,379,325 NDUFA12
    nsv6202016copy number variation1nstd214human GRCh38 chr12: 94,993,269-94,993,395 , GRCh37.p13 chr12: 95,387,045-95,387,171 NDUFA12
    nsv6195525copy number variation1nstd214human GRCh38 chr12: 94,993,231-94,993,366 , GRCh37.p13 chr12: 95,387,007-95,387,142 NDUFA12
    nsv6143764copy number variation1nstd206human GRCh38 chr12: 94,993,270-94,993,353 , GRCh37.p13 chr12: 95,387,046-95,387,129 NDUFA12
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132721copy number variation1nstd213human GRCh37 chr12: 94,820,000-97,270,001 , GRCh38.p12 chr12: 94,426,224-96,876,223 ELK3, METAP2, 50 more genes
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