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Items: 1 to 20 of 367

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7098672copy number variation1nstd102humanUncertain significance GRCh37 chrX: 66,905,832-68,060,497 , GRCh38.p12 chrX: 67,685,990-68,840,654 SERBP1P1, COX6CP12, 14 more genes
    nsv7088448copy number variation1nstd229human GRCh38 chrX: 68,724,869-69,073,808 , GRCh37.p13 chrX: 67,944,711-68,293,651 LOC105373242, STARD8, 4 more genes
    nsv7088447copy number variation1nstd229human GRCh38 chrX: 68,715,368-68,715,531 , GRCh37.p13 chrX: 67,935,210-67,935,373 STARD8
    nsv7088446copy number variation1nstd229human GRCh38 chrX: 68,715,035-68,715,108 , GRCh37.p13 chrX: 67,934,877-67,934,950 STARD8
    nsv7088445copy number variation1nstd229human GRCh38 chrX: 68,709,776-68,712,706 , GRCh37.p13 chrX: 67,929,618-67,932,548 STARD8
    nsv7088444copy number variation1nstd229human GRCh38 chrX: 68,703,129-68,768,567 , GRCh37.p13 chrX: 67,922,971-67,988,410 STARD8
    nsv7088443copy number variation1nstd229human GRCh38 chrX: 68,684,957-68,685,324 , GRCh37.p13 chrX: 67,904,799-67,905,166 STARD8
    nsv7088442copy number variation1nstd229human GRCh38 chrX: 68,673,050-68,675,151 , GRCh37.p13 chrX: 67,892,892-67,894,993 STARD8
    nsv7088441copy number variation1nstd229human GRCh38 chrX: 68,671,109-68,681,868 , GRCh37.p13 chrX: 67,890,951-67,901,710 STARD8
    nsv7088440copy number variation1nstd229human GRCh38 chrX: 68,665,928-68,666,018 , GRCh37.p13 chrX: 67,885,770-67,885,860 STARD8
    nsv7088439copy number variation1nstd229human GRCh38 chrX: 68,656,068-68,656,249 , GRCh37.p13 chrX: 67,875,910-67,876,091 STARD8
    nsv7088438copy number variation1nstd229human GRCh38 chrX: 68,639,830-68,696,351 , GRCh37.p13 chrX: 67,859,672-67,916,193 COX6CP12, STARD8
    nsv7088436copy number variation1nstd229human GRCh38 chrX: 68,623,843-68,655,426 , GRCh37.p13 chrX: 67,843,685-67,875,268 STARD8, COX6CP12
    nsv7088421copy number variation1nstd229human GRCh38 chrX: 68,502,071-68,761,314 , GRCh37.p13 chrX: 67,721,913-67,981,156 RNU6-245P, YIPF6, 3 more genes
    nsv7027510inversion1nstd229human GRCh38 chrX: 68,678,051-68,698,832 , GRCh37.p13 chrX: 67,897,893-67,918,674 STARD8
    nsv7019621inversion1nstd229human GRCh38 chrX: 68,663,808-68,678,250 , GRCh37.p13 chrX: 67,883,650-67,898,092 STARD8
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
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