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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5530293copy number variation1nstd206human GRCh38 chr16: 57,535,703-57,535,780 , GRCh37.p13 chr16: 57,569,615-57,569,692 CCDC102A, ADGRG5
    nsv5305720copy number variation1nstd204human GRCh37.p13 chr16: 57,463,321-57,588,854 , GRCh38.p13 chr16: 57,429,409-57,554,942 POLR2C, DOK4, 4 more genes
    nsv5301175copy number variation1nstd204human GRCh38.p13 chr16: 56,771,413-57,511,371 , GRCh37.p13 chr16: 56,805,325-57,545,283 , PLLP, 24 more genes
    nsv5280053copy number variation1nstd204human GRCh38.p13 chr16: 57,493,039-57,518,678 , GRCh37.p13 chr16: 57,526,951-57,552,590 CCDC102A
    nsv5279384copy number variation1nstd204human GRCh38.p13 chr16: 57,423,301-57,511,300 , GRCh37.p13 chr16: 57,457,213-57,545,212 CCDC102A, CIAPIN1, 3 more genes
    nsv5277685copy number variation1nstd204human GRCh38.p13 chr16: 57,516,929-57,553,397 , GRCh37.p13 chr16: 57,550,841-57,587,309 ADGRG5, CCDC102A
    nsv5005703copy number variation1nstd200human GRCh38 chr16: 57,429,638-57,554,725 , GRCh37.p13 chr16: 57,463,550-57,588,637 DOK4, COQ9, 4 more genes
    nsv4864170copy number variation1nstd200human GRCh37 chr16: 57,463,550-57,588,637 , GRCh38.p12 chr16: 57,429,638-57,554,725 DOK4, POLR2C, 4 more genes
    nsv4864167copy number variation1nstd200human GRCh37 chr16: 56,805,348-57,545,260 , GRCh38.p12 chr16: 56,771,436-57,511,348 , POLR2C, 24 more genes
    nsv4765376insertion1nstd199human GRCh37 chr16: 57,554,448-57,554,448 , GRCh38.p12 chr16: 57,520,536-57,520,536 CCDC102A
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729888copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,292,407-59,103,985 , GRCh38.p12 chr16: 57,258,495-59,070,081 HMGB3P32, DOK4, 57 more genes
    nsv4680656copy number variation1nstd189human GRCh37.p13 chr16: 57,503,346-57,632,795 , GRCh38.p12 chr16: 57,469,434-57,598,883 POLR2C, DOK4, 4 more genes
    nsv4670554copy number variation1nstd186human GRCh37 chr16: 57,570,404-57,570,449 , GRCh38.p12 chr16: 57,536,492-57,536,537 CCDC102A, ADGRG5
    nsv4632886copy number variation1nstd183human GRCh37 chr16: 57,570,016-57,571,105 , GRCh38.p12 chr16: 57,536,104-57,537,193 CCDC102A, ADGRG5
    nsv4628388copy number variation1nstd183human GRCh37 chr16: 57,570,404-57,570,449 , GRCh38.p12 chr16: 57,536,492-57,536,537 CCDC102A, ADGRG5
    nsv4619108copy number variation1nstd183human GRCh37 chr16: 57,570,404-57,570,551 , GRCh38.p12 chr16: 57,536,492-57,536,639 CCDC102A, ADGRG5
    nsv4578617copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,499,814-58,032,169 , GRCh38.p12 chr16: 57,465,902-57,998,265 HMGB3P32, KIFC3, 19 more genes
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
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