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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095026copy number variation2nstd102humanUncertain significance GRCh37 chr16: 49,525,186-51,631,253 , GRCh38.p12 chr16: 49,491,275-51,597,342 RNA5SP426, RPL34P29, 35 more genes
    nsv6995950copy number variation1nstd229human GRCh38 chr16: 50,276,001-50,280,600 , GRCh37.p13 chr16: 50,309,912-50,314,511 ADCY7
    nsv6992224copy number variation1nstd229human GRCh38 chr16: 50,287,483-50,292,578 , GRCh37.p13 chr16: 50,321,394-50,326,489 ADCY7, MIR6771
    nsv6990472copy number variation1nstd229human GRCh38 chr16: 50,317,296-50,317,357 , GRCh37.p13 chr16: 50,351,207-50,351,268 BRD7, ADCY7
    nsv6988549copy number variation1nstd229human GRCh38 chr16: 50,255,744-50,265,125 , GRCh37.p13 chr16: 50,289,655-50,299,036 ADCY7
    nsv6985619copy number variation1nstd229human GRCh38 chr16: 50,268,718-50,277,433 , GRCh37.p13 chr16: 50,302,629-50,311,344 ADCY7
    nsv6984809copy number variation1nstd229human GRCh38 chr16: 50,275,320-50,278,448 , GRCh37.p13 chr16: 50,309,231-50,312,359 ADCY7
    nsv6984336copy number variation1nstd229human GRCh38 chr16: 50,303,465-50,306,734 , GRCh37.p13 chr16: 50,337,376-50,340,645 ADCY7
    nsv6981790copy number variation1nstd229human GRCh38 chr16: 50,284,078-50,299,591 , GRCh37.p13 chr16: 50,317,989-50,333,502 MIR6771, ADCY7
    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
    nsv6634436copy number variation1nstd102humanassociation GRCh37 chr16: 50,089,192-51,652,287 , GRCh38.p12 chr16: 50,055,281-51,618,376 CYLD-AS1, LOC107984892, 29 more genes
    nsv6501683copy number variation1nstd223human GRCh38 chr16: 50,275,315-50,278,442 , GRCh37.p13 chr16: 50,309,226-50,312,353 ADCY7
    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
    nsv6286859insertion1nstd214human GRCh38 chr16: 50,317,296-50,317,296 , GRCh37.p13 chr16: 50,351,207-50,351,207 BRD7, ADCY7
    nsv6145664copy number variation1nstd206human GRCh38 chr16: 50,317,296-50,317,357 , GRCh37.p13 chr16: 50,351,207-50,351,268 ADCY7, BRD7
    nsv6144720copy number variation1nstd206human GRCh38 chr16: 50,280,682-50,307,682 , GRCh37.p13 chr16: 50,314,593-50,341,593 ADCY7, MIR6771
    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
    nsv6088617insertion1nstd212human GRCh38 chr16: 50,252,489-50,252,489 , GRCh37.p13 chr16: 50,286,400-50,286,400 ADCY7
    nsv5651929insertion1nstd207human GRCh38 chr16: 50,317,296-50,317,296 , GRCh37.p13 chr16: 50,351,207-50,351,207 BRD7, ADCY7
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