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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309391copy number variation1nstd102humanPathogenic GRCh37 chr12: 113,120,652-115,362,584 , GRCh38.p12 chr12: 112,682,847-114,924,779 RITA1, LOC105369993, 41 more genes
    nsv6313978copy number variation1nstd102humanPathogenic GRCh37 chr12: 113,445,811-114,933,860 , GRCh38.p12 chr12: 113,008,006-114,496,055 RITA1, LOC105369993, 32 more genes
    nsv3914285copy number variation1nstd102humanPathogenic GRCh38 chr12: 113,077,775-114,372,366 , NCBI36 chr12: 111,999,963-113,294,554 , GRCh37 chr12: 113,515,580-114,810,171 RITA1, DTX1, 27 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 RITA1, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 RITA1, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 RITA1, RNU4ATAC16P, 2452 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 RITA1, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 RITA1, OR5BT1P, 2441 more genes
    nsv6291788copy number variation1nstd102humanLikely benign GRCh37 chr12: 113,622,666-113,848,323 , GRCh38.p12 chr12: 113,184,861-113,410,518 RITA1, SLC8B1, 7 more genes
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