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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968604inversion1nstd209human GRCh38 chr2: 49,436,021-59,087,697 , GRCh37.p13 chr2: 49,663,159-59,314,832 , ACYP2, 95 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5435576copy number variation1nstd206human GRCh38 chr2: 52,262,579-52,623,412 , GRCh37.p13 chr2: 52,489,717-52,850,550 NRXN1-DT, LINC01867, 2 more genes
    nsv5030307inversion1nstd200human GRCh38 chr2: 48,550,793-61,622,055 , GRCh37.p13 chr2: 48,777,932-61,849,190 , MIR217, 146 more genes
    nsv4679580copy number variation1nstd189human GRCh38.p12 chr2: 52,295,827-52,624,828 , GRCh37.p13 chr2: 52,522,965-52,851,966 CRTC1P1, NRXN1-DT, 2 more genes
    nsv4586112copy number variation1nstd183human GRCh37 chr2: 52,599,360-52,759,115 , GRCh38.p12 chr2: 52,372,222-52,531,977 NRXN1-DT, LINC01867, 1 more genes
    nsv4586111copy number variation1nstd183human GRCh37 chr2: 52,572,629-52,660,363 , GRCh38.p12 chr2: 52,345,491-52,433,225 NRXN1-DT, LINC01867
    nsv4398764copy number variation1nstd174human GRCh37 chr2: 52,599,360-52,761,239 , GRCh38.p12 chr2: 52,372,222-52,534,101 GGCTP3, NRXN1-DT, 1 more genes
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
    nsv4331174inversion1nstd166human GRCh37.p13 chr2: 36,139,982-53,112,348 , GRCh38.p12 chr2: 35,914,916-52,885,210 , ASS1P2, 247 more genes
    nsv4057382copy number variation1nstd166human GRCh37.p13 chr2: 52,610,382-52,683,859 , GRCh38.p12 chr2: 52,383,244-52,456,721 NRXN1-DT, LINC01867
    nsv3967841copy number variation1nstd168human GRCh38 chr2: 52,386,335-52,402,772 , GRCh37.p13 chr2: 52,613,473-52,629,910 NRXN1-DT, LINC01867
    nsv3919776copy number variation1nstd102humanUncertain significance NCBI36 chr2: 52,251,568-52,454,647 , GRCh37.p13 chr2: 52,398,064-52,601,143 , GRCh38.p12 chr2: 52,170,926-52,374,005 NRXN1-DT, LINC01867
    nsv3918665copy number variation1nstd102humanUncertain significance NCBI36 chr2: 52,422,551-52,523,982 , GRCh37.p13 chr2: 52,569,047-52,670,478 , GRCh38.p12 chr2: 52,341,909-52,443,340 NRXN1-DT, LINC01867
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3905626copy number variation1nstd102humanPathogenic GRCh37 chr2: 40,965,422-58,090,956 , GRCh38 chr2: 40,738,282-57,863,821 , NCBI36 chr2: 40,818,926-57,944,460 RNU6-433P, RNU6-997P, 220 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3891874copy number variation1nstd102humanPathogenic NCBI36 chr2: 49,991,574-52,542,978 , GRCh37 chr2: 50,138,070-52,689,474 , GRCh38 chr2: 49,910,932-52,462,336 LOC105377627, CRYGGP, 11 more genes
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