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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6923630copy number variation1nstd229human GRCh38 chr12: 49,557,609-49,600,849 , GRCh37.p13 chr12: 49,951,392-49,994,632 PARK7P1, FAM186B, 4 more genes
    nsv6190925copy number variation1nstd214human GRCh38 chr12: 49,564,156-49,564,209 , GRCh37.p13 chr12: 49,957,939-49,957,992 MCRS1
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132250copy number variation1nstd213human GRCh37 chr12: 49,440,000-51,850,001 , GRCh38.p12 chr12: 49,046,217-51,456,217 DAZAP2, KCNH3, 83 more genes
    nsv6032068copy number variation1nstd212human GRCh38 chr12: 49,564,179-49,564,232 , GRCh37.p13 chr12: 49,957,962-49,958,015 MCRS1
    nsv6028833copy number variation1nstd212human GRCh38 chr12: 49,557,048-49,557,109 , GRCh37.p13 chr12: 49,950,831-49,950,892 MCRS1, KCNH3
    nsv5943605copy number variation1nstd209human GRCh38 chr12: 49,553,953-49,564,665 , GRCh37.p13 chr12: 49,947,736-49,958,448 KCNH3, MCRS1
    nsv5935791copy number variation1nstd209human GRCh38 chr12: 49,557,044-49,557,105 , GRCh37.p13 chr12: 49,950,827-49,950,888 MCRS1, KCNH3
    nsv5930969copy number variation1nstd209human GRCh38 chr12: 49,564,156-49,564,209 , GRCh37.p13 chr12: 49,957,939-49,957,992 MCRS1
    nsv5850747copy number variation1nstd209human GRCh38 chr12: 49,553,889-49,564,514 , GRCh37.p13 chr12: 49,947,672-49,958,297 MCRS1, KCNH3
    nsv5513694copy number variation1nstd206human GRCh38 chr12: 49,557,054-49,557,106 , GRCh37.p13 chr12: 49,950,837-49,950,889 MCRS1, KCNH3
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728793copy number variation1nstd102humanUncertain significance GRCh37 chr12: 49,024,019-50,299,974 , GRCh38.p12 chr12: 48,630,236-49,906,191 SPATS2, SPMIP11, 62 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4203112copy number variation1nstd166human GRCh37.p13 chr12: 49,950,837-49,950,889 , GRCh38.p12 chr12: 49,557,054-49,557,106 KCNH3, MCRS1
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
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