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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098218copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,708,675-119,761,021 , GRCh38.p12 chrX: 119,574,712-120,627,166 RHOXF2B, RHOXF1P3, 33 more genes
    nsv7098217copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 117,629,935-119,761,021 , GRCh38.p12 chrX: 118,495,972-120,627,166 HNRNPA1P28, RNU7-86P, 59 more genes
    nsv7083208copy number variation1nstd229human GRCh38 chrX: 119,748,932-120,013,756 , GRCh37.p13 chrX: 118,882,895-119,081,533 RHOXF1P2, RPL39, 11 more genes
    nsv7083197copy number variation1nstd229human GRCh38 chrX: 119,706,101-119,807,400 , GRCh37.p13 chrX: 118,840,064-118,941,363 UPF3B, LOC107985694, 3 more genes
    nsv7083190copy number variation1nstd229human GRCh38 chrX: 119,649,601-119,807,300 , GRCh37.p13 chrX: 118,783,564-118,941,263 SEPTIN6, LOC107985694, 4 more genes
    nsv7083184copy number variation1nstd229human GRCh38 chrX: 119,593,801-119,978,300 , GRCh37.p13 chrX: 118,727,764-119,081,533 NKRF, SOWAHD, 11 more genes
    nsv7083182copy number variation1nstd229human GRCh38 chrX: 119,575,201-119,955,200 , GRCh37.p13 chrX: 118,709,164-119,081,533 RPL39, MIR766, 12 more genes
    nsv7083176copy number variation1nstd229human GRCh38 chrX: 119,469,701-119,803,000 , GRCh37.p13 chrX: 118,603,664-118,936,963 SLC25A5, LOC107985694, 8 more genes
    nsv7083165copy number variation1nstd229human GRCh38 chrX: 119,399,501-119,803,000 , GRCh37.p13 chrX: 118,533,464-118,936,963 SLC25A43, SOWAHD, 13 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7053551inversion1nstd229human GRCh38 chrX: 119,787,766-120,266,058 , GRCh37.p13 chrX|NW_004070886.1: 1-318,488 , GRCh37.p13 chrX: 119,081,534-119,399,913 TMEM255A, RHOXF2B, 20 more genes
    nsv7053106inversion1nstd229human GRCh38 chrX: 118,857,141-120,493,178 , GRCh37.p13 chrX: 117,991,104-119,627,033 LINC03098, RNF113A, 49 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7040757inversion1nstd229human GRCh38 chrX: 119,358,756-119,946,578 , GRCh37.p13 chrX: 118,492,719-119,080,541 NDUFA1, UBE2A, 20 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 more genes
    nsv6636610copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,718,147-119,128,855 , GRCh38.p12 chrX: 119,584,184-119,994,892 LOC107985694, NDUFA1, 13 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6633963copy number variation1nstd224human GRCh37 chrX: 118,763,453-119,037,260 , GRCh38.p12 chrX: 119,629,490-119,903,297 RPL39, LOC100422368, 9 more genes
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