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Items: 1 to 20 of 518

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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
    nsv7081239copy number variation1nstd229human GRCh38 chrX: 56,815,053-56,821,736 , GRCh37.p13 chrX: 56,841,486-56,848,169 NBDY
    nsv7081238copy number variation1nstd229human GRCh38 chrX: 56,802,048-56,803,110 , GRCh37.p13 chrX: 56,828,481-56,829,543 NBDY
    nsv7081237copy number variation1nstd229human GRCh38 chrX: 56,791,297-56,799,255 , GRCh37.p13 chrX: 56,817,730-56,825,688 NBDY
    nsv7081236copy number variation1nstd229human GRCh38 chrX: 56,766,755-56,766,994 , GRCh37.p13 chrX: 56,793,188-56,793,427 NBDY
    nsv7081235copy number variation1nstd229human GRCh38 chrX: 56,752,465-56,758,359 , GRCh37.p13 chrX: 56,778,898-56,784,792 NBDY
    nsv7081234copy number variation1nstd229human GRCh38 chrX: 56,745,439-56,810,734 , GRCh37.p13 chrX: 56,771,872-56,837,167 NBDY
    nsv7081233copy number variation1nstd229human GRCh38 chrX: 56,736,341-56,737,194 , GRCh37.p13 chrX: 56,762,774-56,763,627 NBDY, UQCRBP1
    nsv7081232copy number variation1nstd229human GRCh38 chrX: 56,736,301-57,097,000 , GRCh37.p13 chrX: 56,762,734-57,123,433 SPIN3, SPIN2P1, 2 more genes
    nsv7081231copy number variation1nstd229human GRCh38 chrX: 56,728,281-56,728,510 , GRCh37.p13 chrX: 56,754,714-56,754,943 NBDY
    nsv7081230copy number variation1nstd229human GRCh38 chrX: 56,726,083-56,731,574 , GRCh37.p13 chrX: 56,752,516-56,758,007 NBDY
    nsv7081185copy number variation1nstd229human GRCh38 chrX: 56,564,882-57,142,271 , GRCh37.p13 chrX: 56,591,315-57,168,704 FAAH2, NBDY, 6 more genes
    nsv7027846inversion1nstd229human GRCh38 chrX: 56,755,071-57,478,649 , GRCh37.p13 chrX: 56,781,504-57,505,082 MTHFD1P1, PPP1R11P2, 6 more genes
    nsv7025237inversion1nstd229human GRCh38 chrX: 50,557,525-57,228,328 , GRCh37.p13 chrX|NW_004070877.1: 270,640-4,110,759 , GRCh37.p13 chrX: 50,300,525-54,424,077 UBQLN2, IPO7P1, 141 more genes
    nsv7024182inversion1nstd229human GRCh38 chrX: 55,283,275-57,909,590 , GRCh37.p13 chrX: 55,309,708-57,936,024 UBQLN2, USP51, 27 more genes
    nsv7020530inversion1nstd229human GRCh38 chrX: 56,736,354-57,752,027 , GRCh37.p13 chrX: 56,762,787-57,778,460 UQCRBP1, LOC107985708, 10 more genes
    nsv6636248copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 53,731,940-63,932,866 , GRCh38.p12 chrX: 53,704,997-64,712,986 ALAS2, FGD1, 89 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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