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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv425657insertion1nstd6human NCBI35 chrX: 37,607,190-37,607,190 , GRCh37.p13 chrX: 37,850,973-37,850,973 , GRCh38.p12 chrX: 37,991,720-37,991,720 SYTL5, H2AP
    nsv425656insertion1nstd6human NCBI35 chrX: 37,606,898-37,606,898 , GRCh37.p13 chrX: 37,850,681-37,850,681 , GRCh38.p12 chrX: 37,991,428-37,991,428 SYTL5, H2AP
    nsv2684992short tandem repeat1nstd128human GRCh37 chrX: 37,849,293-37,849,319 , GRCh38.p12 chrX: 37,990,040-37,990,066 SYTL5, H2AP
    nsv2668325short tandem repeat1nstd128human GRCh37 chrX: 37,849,124-37,849,140 , GRCh38.p12 chrX: 37,989,871-37,989,887 SYTL5, H2AP
    nsv3893063copy number variation1nstd102humanLikely benign NCBI36 chrX: 37,699,670-37,864,547 , GRCh37 chrX: 37,814,726-37,979,603 , GRCh38 chrX: 37,955,473-38,120,350 MIR548AJ2, SYTL5, 2 more genes
    nsv3880207copy number variation1nstd102humanUncertain significance GRCh37 chrX: 37,810,186-37,879,337 , GRCh38.p12 chrX: 37,950,933-38,020,084 SYTL5, H2AL3, 1 more genes
    nsv7080747copy number variation1nstd229human GRCh38 chrX: 37,948,032-38,020,160 , GRCh37.p13 chrX: 37,807,285-37,879,413 H2AL3, SYTL5, 1 more genes
    nsv7080749copy number variation1nstd229human GRCh38 chrX: 37,991,501-38,000,107 , GRCh37.p13 chrX: 37,850,754-37,859,360 SYTL5, H2AP, 1 more genes
    nsv7080748copy number variation1nstd229human GRCh38 chrX: 37,990,676-37,992,422 , GRCh37.p13 chrX: 37,849,929-37,851,675 H2AP, H2AL3, 1 more genes
    nsv5887433copy number variation1nstd209human GRCh38 chrX: 37,991,457-37,995,172 , GRCh37.p13 chrX: 37,850,710-37,854,425 H2AP, SYTL5, 1 more genes
    nsv4633946copy number variation1nstd183human GRCh37 chrX: 37,850,770-37,854,365 , GRCh38.p12 chrX: 37,991,517-37,995,112 H2AP, SYTL5, 1 more genes
    nsv4417093copy number variation1nstd174human GRCh37 chrX: 37,850,770-37,854,621 , GRCh38.p12 chrX: 37,991,517-37,995,368 H2AP, SYTL5, 1 more genes
    esv2675672copy number variation15estd199human GRCh37 chrX: 37,850,770-37,854,365 , GRCh38.p12 chrX: 37,991,517-37,995,112 H2AP, SYTL5, 1 more genes
    nsv424909copy number variation1nstd6human NCBI35 chrX: 37,607,243-37,610,838 , GRCh37.p13 chrX: 37,851,026-37,854,621 , GRCh38.p12 chrX: 37,991,773-37,995,368 H2AP, SYTL5, 1 more genes
    nsv5428311copy number variation1nstd206human GRCh38 chrX: 37,954,342-37,996,937 , GRCh37.p13 chrX: 37,813,595-37,856,190 H2AL3, H2AP, 1 more genes
    nsv5430366copy number variation1nstd206human GRCh38 chrX: 37,991,514-37,995,010 , GRCh37.p13 chrX: 37,850,767-37,854,263 H2AP, SYTL5, 1 more genes
    esv3888705copy number variation1estd219human GRCh37 chrX: 37,813,162-37,855,992 , GRCh38.p12 chrX: 37,953,909-37,996,739 H2AL3, H2AP, 1 more genes
    nsv518029copy number variation1nstd21human NCBI35 chrX: 37,546,199-37,754,231 , GRCh37.p13 chrX: 37,789,982-37,998,014 , GRCh38.p12 chrX: 37,930,729-38,138,761 SC4MOP, H2AP, 3 more genes
    nsv519012copy number variation1nstd21human NCBI35 chrX: 37,591,385-37,668,492 , GRCh37.p13 chrX: 37,835,168-37,912,275 , GRCh38.p12 chrX: 37,975,915-38,053,022 H2AP, SYTL5, 2 more genes
    nsv432319copy number variation1nstd12human NCBI35 chrX: 37,546,100-37,732,300 , GRCh37.p13 chrX: 37,789,883-37,976,083 , GRCh38.p12 chrX: 37,930,630-38,116,830 SC4MOP, H2AP, 3 more genes
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