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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5597233copy number variation1nstd207human GRCh38 chr10: 67,784,403-67,795,563 , GRCh37.p13 chr10: 69,544,161-69,555,321 DNAJC12, RPL21P92
    nsv5482449copy number variation1nstd206human GRCh38 chr10: 67,784,939-67,795,564 , GRCh37.p13 chr10: 69,544,697-69,555,322 RPL21P92, DNAJC12
    nsv5478614copy number variation1nstd206human GRCh38 chr10: 67,789,542-67,799,755 , GRCh37.p13 chr10: 69,549,300-69,559,513 DNAJC12, RPL21P92
    nsv5310299copy number variation1nstd204human GRCh37.p13 chr10: 69,544,673-69,555,344 , GRCh38.p13 chr10: 67,784,915-67,795,586 DNAJC12, RPL21P92
    nsv5248839copy number variation1nstd204human GRCh38.p13 chr10: 67,783,926-67,795,540 , GRCh37.p13 chr10: 69,543,684-69,555,298 RPL21P92, DNAJC12
    nsv5242251copy number variation1nstd204human GRCh38.p13 chr10: 67,784,101-67,795,600 , GRCh37.p13 chr10: 69,543,859-69,555,358 DNAJC12, RPL21P92
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976322copy number variation1nstd200human GRCh38 chr10: 67,784,939-67,795,564 , GRCh37.p13 chr10: 69,544,697-69,555,322 RPL21P92, DNAJC12
    nsv4838849copy number variation1nstd200human GRCh37 chr10: 69,544,697-69,555,322 , GRCh38.p12 chr10: 67,784,939-67,795,564 RPL21P92, DNAJC12
    nsv4675581copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,066,516-70,079,295 , GRCh38.p12 chr10: 67,306,758-68,319,538 RN7SL220P, TRS-TGA1-1, 22 more genes
    nsv4675035copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,545,126-69,883,765 , GRCh38.p12 chr10: 67,785,368-68,124,008 POU5F1P5, RN7SL394P, 11 more genes
    nsv4614284copy number variation1nstd183human GRCh37 chr10: 69,544,696-69,555,322 , GRCh38.p12 chr10: 67,784,938-67,795,564 DNAJC12, RPL21P92
    nsv4427929copy number variation1nstd174human GRCh37 chr10: 69,544,696-69,559,538 , GRCh38.p12 chr10: 67,784,938-67,799,780 DNAJC12, RPL21P92
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4180759copy number variation1nstd166human GRCh37.p13 chr10: 69,263,643-70,077,786 , GRCh38.p12 chr10: 67,503,885-68,318,029 RPL21P92, RNU6-1250P, 20 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 MYL6P3, CHCHD1, 220 more genes
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