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Items: 1 to 20 of 37

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3894784copy number variation1nstd102humanUncertain significance GRCh37 chr15: 57,711,740-57,749,246 , GRCh38.p12 chr15: 57,419,542-57,457,048 CGNL1
    nsv3904704copy number variation1nstd102humanBenign GRCh37 chr15: 57,644,456-57,775,826 , GRCh38.p12 chr15: 57,352,258-57,483,628 CGNL1, RNU6-844P
    nsv3890570copy number variation1nstd102humanBenign GRCh37 chr15: 57,644,656-57,775,826 , GRCh38.p12 chr15: 57,352,458-57,483,628 CGNL1, RNU6-844P
    nsv3906865copy number variation1nstd102humanBenign GRCh37 chr15: 57,645,324-57,775,826 , GRCh38.p12 chr15: 57,353,126-57,483,628 CGNL1, RNU6-844P
    nsv3898296copy number variation1nstd102humanBenign GRCh37 chr15: 57,645,569-57,775,826 , GRCh38.p12 chr15: 57,353,371-57,483,628 CGNL1, RNU6-844P
    nsv3923096copy number variation1nstd102humanBenign NCBI36 chr15: 55,443,297-55,535,566 , GRCh37 chr15: 57,656,005-57,748,274 , GRCh38 chr15: 57,363,807-57,456,076 CGNL1, RNU6-844P
    nsv3911884copy number variation1nstd102humanUncertain significance GRCh37 chr15: 57,667,027-57,734,290 , GRCh38 chr15: 57,374,829-57,442,092 CGNL1, RNU6-844P
    nsv3908567copy number variation1nstd102humanUncertain significance GRCh37 chr15: 57,687,531-57,825,782 , GRCh38.p12 chr15: 57,395,333-57,533,584 CGNL1, RNU6-844P, 1 more genes
    nsv3897890copy number variation1nstd102humanUncertain significance GRCh37 chr15: 57,759,358-57,880,518 , GRCh38.p12 chr15: 57,467,160-57,588,320 CGNL1, RPS13P7, 1 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 CGNL1, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 CGNL1, RNU6-18P, 1442 more genes
    nsv3913164copy number variation1nstd102humanPathogenic GRCh38 chr15: 50,864,913-59,646,577 , GRCh37 chr15: 51,157,110-59,938,776 , NCBI36 chr15: 48,944,402-57,726,068 CGNL1, LOC112268148, 131 more genes
    nsv3899878copy number variation1nstd102humanPathogenic GRCh37 chr15: 54,713,558-62,769,295 , GRCh38.p12 chr15: 54,421,360-62,477,096 CGNL1, RAB27A, 120 more genes
    nsv3913143copy number variation1nstd102humanPathogenic GRCh38 chr15: 57,456,076-61,907,285 , GRCh37 chr15: 57,748,274-62,199,484 , NCBI36 chr15: 55,535,566-59,986,776 CGNL1, HMGB1P51, 73 more genes
    nsv6291481copy number variation1nstd102humanPathogenic GRCh37 chr15: 55,772,371-57,880,518 , GRCh38.p12 chr15: 55,480,173-57,588,320 CGNL1, PRTG, 27 more genes
    nsv7094391copy number variation1nstd102humanPathogenic GRCh37 chr15: 56,961,021-57,839,688 , GRCh38.p12 chr15: 56,668,823-57,547,490 CGNL1, ZNF280D, 11 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 CGNL1, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 CGNL1, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 CGNL1, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 CGNL1, FES, 1738 more genes
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