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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148069copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 118,544,103-118,676,607 , GRCh38.p12 chrX: 119,410,140-119,542,644 SLC25A5, STEEP1, 5 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
    nsv7098847copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,533,367-118,679,467 , GRCh38.p12 chrX: 119,399,404-119,545,504 SLC25A5-AS1, SLC25A5, 5 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
    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
    nsv7083175copy number variation1nstd229human GRCh38 chrX: 119,464,537-119,530,780 , GRCh37.p13 chrX: 118,598,500-118,664,743 SLC25A5-AS1, SLC25A5
    nsv7083174copy number variation1nstd229human GRCh38 chrX: 119,463,601-119,476,000 , GRCh37.p13 chrX: 118,597,564-118,609,963 SLC25A5, SLC25A5-AS1
    nsv7083173copy number variation1nstd229human GRCh38 chrX: 119,454,729-119,475,141 , GRCh37.p13 chrX: 118,588,692-118,609,104 SLC25A5-AS1, RNY3P16, 2 more genes
    nsv7083172copy number variation1nstd229human GRCh38 chrX: 119,453,123-119,677,105 , GRCh37.p13 chrX: 118,587,086-118,811,068 SLC25A43, NKRF, 7 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
    nsv7083158copy number variation1nstd229human GRCh38 chrX: 119,361,411-119,565,034 , GRCh37.p13 chrX: 118,495,374-118,698,997 STEEP1, SLC25A43, 6 more genes
    nsv7083100copy number variation1nstd229human GRCh38 chrX: 119,244,582-119,503,676 , GRCh37.p13 chrX: 118,378,545-118,637,639 SLC25A5-AS1, SLC25A5, 8 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
    nsv7055271inversion1nstd229human GRCh38 chrX: 114,091,775-119,749,531 , GRCh37.p13 chrX: 115,732,291-118,883,494 ZCCHC12, CT47C1, 83 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
    nsv6637078copy number variation1nstd102humanUncertain significance GRCh37 chrX: 117,651,370-118,792,490 , GRCh38.p12 chrX: 118,517,407-119,658,527 LONRF3, CT47C1, 28 more genes
    nsv6636816copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,498,236-118,804,983 , GRCh38.p12 chrX: 119,364,273-119,671,020 SLC25A5, RNY3P16, 10 more genes
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