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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978023insertion1nstd209human GRCh38 chr13: 105,483,405-105,483,405 , GRCh37.p13 chr13: 106,135,754-106,135,754 DAOA-AS1, DAOA
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5006813copy number variation1nstd200human GRCh38 chr13: 105,474,586-105,475,586 , GRCh37.p13 chr13: 106,126,935-106,127,935 DAOA-AS1, DAOA
    nsv5006812copy number variation1nstd200human GRCh38 chr13: 105,467,114-105,469,939 , GRCh37.p13 chr13: 106,119,463-106,122,288 DAOA, DAOA-AS1
    nsv4873007inversion1nstd200human GRCh37 chr13: 103,691,176-106,927,502 , GRCh38.p12 chr13: 103,038,826-106,275,153 LINC01309, LOC107984607, 19 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4848282copy number variation1nstd200human GRCh37 chr13: 106,126,935-106,127,935 , GRCh38.p12 chr13: 105,474,586-105,475,586 DAOA, DAOA-AS1
    nsv4729283copy number variation1nstd102humanUncertain significance GRCh37 chr13: 104,340,651-106,143,116 , GRCh38.p12 chr13: 103,688,301-105,490,767 LOC107984608, DAOA-AS1, 10 more genes
    nsv4728886copy number variation1nstd102humanUncertain significance GRCh37 chr13: 106,080,968-106,748,711 , GRCh38.p12 chr13: 105,428,619-106,096,362 DAOA-AS1, LOC105370345, 2 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4680435copy number variation1nstd189human GRCh37.p13 chr13: 104,580,717-106,705,915 , GRCh38.p12 chr13: 103,928,367-106,053,566 LINC00343, DAOA, 12 more genes
    nsv4675882copy number variation1nstd102humanPathogenic GRCh37 chr13: 104,521,177-109,327,788 , GRCh38.p12 chr13: 103,868,827-108,604,133 LOC107984608, LOC105370353, 39 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    nsv4675169copy number variation1nstd102humanUncertain significance GRCh37 chr13: 106,041,979-106,206,419 , GRCh38.p12 chr13: 105,389,629-105,554,070 LOC105370344, DAOA, 1 more genes
    nsv4612266copy number variation1nstd183human GRCh37 chr13: 106,120,419-106,133,485 , GRCh38.p12 chr13: 105,468,070-105,481,136 DAOA-AS1, DAOA
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4456260copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258 F10, FKSG29, 300 more genes
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