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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
    nsv7098567copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 73,641,473-74,376,107 , GRCh38.p12 chrX: 74,421,638-75,156,272 ABCB7, SLC16A2, 6 more genes
    nsv7088881copy number variation1nstd229human GRCh38 chrX: 75,143,436-75,143,820 , GRCh37.p13 chrX: 74,363,271-74,363,655 ABCB7
    nsv7088880copy number variation1nstd229human GRCh38 chrX: 75,104,064-75,104,086 , GRCh37.p13 chrX: 74,323,899-74,323,921 ABCB7
    nsv7088879copy number variation1nstd229human GRCh38 chrX: 75,096,465-75,096,536 , GRCh37.p13 chrX: 74,316,300-74,316,371 ABCB7
    nsv7088878copy number variation1nstd229human GRCh38 chrX: 75,087,401-75,105,600 , GRCh37.p13 chrX: 74,307,236-74,325,435 ABCB7
    nsv7088877copy number variation1nstd229human GRCh38 chrX: 75,083,576-75,088,616 , GRCh37.p13 chrX: 74,303,411-74,308,451 ABCB7
    nsv7088876copy number variation1nstd229human GRCh38 chrX: 75,079,247-75,088,615 , GRCh37.p13 chrX: 74,299,082-74,308,450 ABCB7
    nsv7088875copy number variation1nstd229human GRCh38 chrX: 75,079,246-75,083,520 , GRCh37.p13 chrX: 74,299,081-74,303,355 ABCB7
    nsv7088874copy number variation1nstd229human GRCh38 chrX: 75,062,501-75,110,600 , GRCh37.p13 chrX: 74,282,336-74,330,435 ABCB7
    nsv7088873copy number variation1nstd229human GRCh38 chrX: 75,062,501-75,067,100 , GRCh37.p13 chrX: 74,282,336-74,286,935 ABCB7
    nsv7088872copy number variation1nstd229human GRCh38 chrX: 75,040,071-75,051,218 , GRCh37.p13 chrX: 74,259,906-74,271,053 ABCB7
    nsv7088859copy number variation1nstd229human GRCh38 chrX: 74,918,273-75,426,908 , GRCh37.p13 chrX: 74,138,108-74,646,743 NEXMIF, RPL21P134, 6 more genes
    nsv7033124inversion1nstd229human GRCh38 chrX: 75,136,136-75,136,171 , GRCh37.p13 chrX: 74,355,971-74,356,006 ABCB7
    nsv7027122inversion1nstd229human GRCh38 chrX: 74,878,735-76,069,015 , GRCh37.p13 chrX: 74,098,570-75,200,415 TERF1P7, ZDHHC15, 13 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
    nsv6637085copy number variation1nstd102humanUncertain significance GRCh37 chrX: 74,255,362-74,509,925 , GRCh38.p12 chrX: 75,035,527-75,290,090 RNU6-562P, BUD31P2, 2 more genes
    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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