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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729919copy number variation1nstd102humanUncertain significance GRCh37 chr16: 86,287,540-86,718,579 , GRCh38.p12 chr16: 86,253,934-86,684,973 FENDRR, FOXC2-AS1, 10 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4674955copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,872,102-87,678,641 , GRCh38.p12 chr16: 84,838,496-87,645,035 RPL7AP63, LOC105371388, 62 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4374540copy number variation1nstd173human GRCh37 chr16: 86,359,211-86,665,459 , GRCh38.p12 chr16: 86,325,605-86,631,853 RPL7AP63, LINC00917, 8 more genes
    nsv4373011copy number variation1nstd173human GRCh37 chr16: 85,070,511-86,960,204 , GRCh38.p12 chr16: 85,036,905-86,926,598 , LOC101928502, 46 more genes
    nsv4349253copy number variation1nstd102humanPathogenic GRCh37 chr16: 82,761,333-90,055,381 , GRCh38.p12 chr16: 82,727,728-89,988,973 RN7SL134P, CDK10, 178 more genes
    nsv3971864copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 86,600,942-86,602,447 , GRCh38 chr16: 86,567,336-86,568,841 FOXC2, FOXC2-AS1
    nsv3922890copy number variation1nstd102humanPathogenic GRCh37 chr16: 70,783,301-90,163,403 , GRCh38 chr16: 70,749,398-90,096,995 , NCBI36 chr16: 69,340,802-88,690,904 GCSH, LOC390739, 362 more genes
    nsv3922616copy number variation1nstd102humanPathogenic GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393 FOXF1, RNA5SP431, 367 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3919844copy number variation1nstd102humanPathogenic GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449 RPL10AP12, LINC01082, 146 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 LOC105376772, WWP2, 527 more genes
    nsv3918765copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 82,579,676-88,675,894 , GRCh37 chr16: 84,022,175-90,148,393 , GRCh38 chr16: 83,988,570-90,081,985 AFG3L1P, APRT, 172 more genes
    nsv3918297copy number variation1nstd102humanPathogenic GRCh38 chr16: 76,336,203-90,088,654 , NCBI36 chr16: 74,927,601-88,682,563 , GRCh37 chr16: 76,370,100-90,155,062 SYCE1L, RN7SL381P, 253 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3917369copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 82,069,559-88,526,819 , GRCh37 chr16: 83,512,058-89,999,318 , GRCh38 chr16: 83,478,453-89,932,910 APRT, CA5A, 170 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
    nsv3916543copy number variation1nstd102humanPathogenic GRCh37 chr16: 75,411,879-90,148,400 , NCBI36 chr16: 73,969,380-88,675,901 , GRCh38 chr16: 75,377,981-90,081,992 MLYCD, RPL7AP63, 274 more genes
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