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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv6992802copy number variation1nstd229human GRCh38 chr16: 57,415,901-57,529,100 , GRCh37.p13 chr16: 57,449,813-57,563,012 DOK4, COQ9, 5 more genes
    nsv6987003copy number variation1nstd229human GRCh38 chr16: 57,446,492-57,489,125 , GRCh37.p13 chr16: 57,480,404-57,523,037 COQ9, DOK4, 2 more genes
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 more genes
    nsv6978535copy number variation1nstd229human GRCh38 chr16: 57,188,715-57,538,791 , GRCh37.p13 chr16: 57,222,627-57,572,703 CX3CL1, ARL2BP, 13 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    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
    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
    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
    nsv5261652copy number variation1nstd204human GRCh38.p13 chr16: 57,429,216-57,460,619 , GRCh37.p13 chr16: 57,463,128-57,494,531 COQ9, CIAPIN1
    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
    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
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