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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142536copy number variation1nstd232human GRCh37.p13 chr12: 49,717,534-49,717,625 , GRCh38.p12 chr12: 49,323,751-49,323,842 TROAP, TROAP-AS1
    nsv6936270copy number variation1nstd229human GRCh38 chr12: 49,323,206-49,327,919 , GRCh37.p13 chr12: 49,716,989-49,721,702 TROAP-AS1, TROAP
    nsv6919792copy number variation1nstd229human GRCh38 chr12: 49,329,289-49,336,312 , GRCh37.p13 chr12: 49,723,072-49,730,095 C1QL4, TROAP
    nsv6470465copy number variation1nstd223human GRCh38 chr12: 49,321,640-49,322,257 , GRCh37.p13 chr12: 49,715,423-49,716,040 TROAP-AS1, TROAP
    nsv6464874copy number variation1nstd223human GRCh38 chr12: 49,323,206-49,327,915 , GRCh37.p13 chr12: 49,716,989-49,721,698 TROAP, TROAP-AS1
    nsv6460469copy number variation1nstd223human GRCh38 chr12: 49,319,931-49,322,679 , GRCh37.p13 chr12: 49,713,714-49,716,462 TROAP-AS1, TROAP
    nsv6198044copy number variation1nstd214human GRCh38 chr12: 49,330,530-49,330,628 , GRCh37.p13 chr12: 49,724,313-49,724,411 TROAP, C1QL4
    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
    nsv6020648copy number variation1nstd212human GRCh38 chr12: 49,330,561-49,330,659 , GRCh37.p13 chr12: 49,724,344-49,724,442 C1QL4, TROAP
    nsv5864604copy number variation1nstd209human GRCh38 chr12: 49,326,472-49,327,671 , GRCh37.p13 chr12: 49,720,255-49,721,454 TROAP
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4972571copy number variation1nstd200human GRCh38 chr12: 49,321,640-49,322,257 , GRCh37.p13 chr12: 49,715,423-49,716,040 TROAP-AS1, TROAP
    nsv4831183copy number variation1nstd200human GRCh37 chr12: 49,715,423-49,716,040 , GRCh38.p12 chr12: 49,321,640-49,322,257 TROAP, TROAP-AS1
    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
    nsv4728980copy number variation1nstd102humanUncertain significance GRCh37 chr12: 49,584,942-49,910,016 , GRCh38.p12 chr12: 49,191,159-49,516,233 LOC100335030, TROAP-AS1, 6 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
    nsv4386064copy number variation1nstd173human GRCh37 chr12: 49,555,059-49,816,495 , GRCh38.p12 chr12: 49,161,276-49,422,712 TROAP, SPATS2, 7 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
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