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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068141inversion1nstd229human GRCh38 chr16: 56,038,949-56,473,255 , GRCh37.p13 chr16: 56,072,861-56,507,167 AMFR, GNAO1-DT, 9 more genes
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv6997846copy number variation1nstd229human GRCh38 chr16: 56,119,601-56,127,200 , GRCh37.p13 chr16: 56,153,513-56,161,112 LOC102725116, GNAO1-DT
    nsv6988150copy number variation1nstd229human GRCh38 chr16: 55,483,186-56,126,631 , GRCh37.p13 chr16: 55,517,098-56,160,543 CES1P1, LOC105371280, 11 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6637389copy number variation1nstd102humanUncertain significance GRCh37 chr16: 55,723,839-56,330,832 , GRCh38.p12 chr16: 55,689,927-56,296,920 LOC107984815, MIR3935, 11 more genes
    nsv6502034copy number variation1nstd223human GRCh38 chr16: 56,130,267-56,130,666 , GRCh37.p13 chr16: 56,164,179-56,164,578 LOC102725116, GNAO1-DT
    nsv6501660copy number variation1nstd223human GRCh38 chr16: 56,133,230-56,133,911 , GRCh37.p13 chr16: 56,167,142-56,167,823 GNAO1-DT, LOC102725116
    nsv6498845copy number variation1nstd223human GRCh38 chr16: 56,131,367-56,131,883 , GRCh37.p13 chr16: 56,165,279-56,165,795 LOC102725116, GNAO1-DT
    nsv6498050copy number variation1nstd223human GRCh38 chr16: 56,119,607-56,127,169 , GRCh37.p13 chr16: 56,153,519-56,161,081 LOC102725116, GNAO1-DT
    nsv6497713copy number variation1nstd223human GRCh38 chr16: 56,113,659-56,114,139 , GRCh37.p13 chr16: 56,147,571-56,148,051 GNAO1-DT, LOC102725116
    nsv6496176copy number variation1nstd223human GRCh38 chr16: 56,114,907-56,115,540 , GRCh37.p13 chr16: 56,148,819-56,149,452 LOC102725116, GNAO1-DT
    nsv6315493copy number variation1nstd102humanPathogenic GRCh37 chr16: 55,054,348-56,403,200 , GRCh38.p12 chr16: 55,020,436-56,369,288 LOC102725116, LOC105371281, 21 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6025340copy number variation1nstd212human GRCh38 chr16: 56,136,910-56,136,992 , GRCh37.p13 chr16: 56,170,822-56,170,904 LOC102725116, GNAO1-DT
    nsv5358209translocation1nstd200human GRCh38 chr16: 56,128,909-56,128,909 , GRCh38 chr16: 56,128,853-56,128,853 , GRCh37.p13 chr16: 56,162,765-56,162,765 , GRCh37.p13 chr16: 56,162,821-56,162,821 LOC102725116, GNAO1-DT
    nsv5358207translocation1nstd200human GRCh38 chr16: 56,107,145-56,107,145 , GRCh38 chr16: 56,107,208-56,107,208 , GRCh37.p13 chr16: 56,141,120-56,141,120 , GRCh37.p13 chr16: 56,141,057-56,141,057 LOC102725116, GNAO1-DT
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