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Items: 1 to 20 of 575

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138845insertion1nstd232human GRCh37.p13 chrX: 74,928,698-74,928,698 , GRCh38.p12 chrX: 75,708,863-75,708,863 LOC107985664
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7088937copy number variation1nstd229human GRCh38 chrX: 75,783,401-75,789,300 , GRCh37.p13 chrX: 75,003,236-75,009,135 LOC107985664, MAGEE2
    nsv7088936copy number variation1nstd229human GRCh38 chrX: 75,778,159-75,778,373 , GRCh37.p13 chrX: 74,997,994-74,998,208 LOC107985664
    nsv7088935copy number variation1nstd229human GRCh38 chrX: 75,759,301-75,761,400 , GRCh37.p13 chrX: 74,979,136-74,981,235 LOC107985664
    nsv7088934copy number variation1nstd229human GRCh38 chrX: 75,747,071-75,747,131 , GRCh37.p13 chrX: 74,966,906-74,966,966 LOC107985664
    nsv7088933copy number variation1nstd229human GRCh38 chrX: 75,724,001-75,779,500 , GRCh37.p13 chrX: 74,943,836-74,999,335 TTC3P1, LOC107985664
    nsv7088932copy number variation1nstd229human GRCh38 chrX: 75,719,155-75,721,924 , GRCh37.p13 chrX: 74,938,990-74,941,759 LOC107985664
    nsv7088931copy number variation1nstd229human GRCh38 chrX: 75,714,401-75,779,500 , GRCh37.p13 chrX: 74,934,236-74,999,335 TTC3P1, LOC107985664
    nsv7088930copy number variation1nstd229human GRCh38 chrX: 75,708,660-75,713,463 , GRCh37.p13 chrX: 74,928,495-74,933,298 LOC107985664
    nsv7088929copy number variation1nstd229human GRCh38 chrX: 75,700,906-75,703,772 , GRCh37.p13 chrX: 74,920,741-74,923,607 LOC107985664
    nsv7088928copy number variation1nstd229human GRCh38 chrX: 75,683,137-75,686,509 , GRCh37.p13 chrX: 74,902,972-74,906,344 LOC107985664
    nsv7088927copy number variation1nstd229human GRCh38 chrX: 75,680,501-75,683,000 , GRCh37.p13 chrX: 74,900,336-74,902,835 LOC107985664
    nsv7088926copy number variation1nstd229human GRCh38 chrX: 75,677,512-76,120,400 , GRCh37.p13 chrX: 74,897,347-75,200,415 ARL5AP5, MAGEE2, 3 more genes
    nsv7088925copy number variation1nstd229human GRCh38 chrX: 75,664,173-75,665,760 , GRCh37.p13 chrX: 74,884,008-74,885,595 LOC107985664
    nsv7088924copy number variation1nstd229human GRCh38 chrX: 75,659,718-75,660,099 , GRCh37.p13 chrX: 74,879,553-74,879,934 LOC107985664
    nsv7088923copy number variation1nstd229human GRCh38 chrX: 75,638,295-75,642,447 , GRCh37.p13 chrX: 74,858,130-74,862,282 LOC107985664
    nsv7088922copy number variation1nstd229human GRCh38 chrX: 75,628,420-75,630,560 , GRCh37.p13 chrX: 74,848,255-74,850,395 LOC107985664
    nsv7088921copy number variation1nstd229human GRCh38 chrX: 75,620,051-76,168,081 , GRCh37.p13 chrX: 74,839,886-75,200,415 ARL5AP5, MAGEE2, 3 more genes
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