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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923742copy number variation1nstd209human GRCh38 chr12: 21,398,810-28,763,815 , GRCh37.p13 chr12: 21,551,744-28,916,748 , LOC105369710, 101 more genes
    nsv5916901copy number variation1nstd209human GRCh38 chr12: 21,398,719-28,763,765 , GRCh37.p13 chr12: 21,551,653-28,916,698 , LOC105369704, 101 more genes
    nsv5849806copy number variation1nstd209human GRCh38 chr12: 24,702,750-24,705,299 , GRCh37.p13 chr12: 24,855,684-24,858,233 LOC105369698, RN7SL38P
    nsv4974448copy number variation1nstd200human GRCh38 chr12: 24,581,434-25,314,724 , GRCh37.p13 chr12: 24,734,368-25,467,658 , LOC105369699, 15 more genes
    nsv4974447copy number variation1nstd200human GRCh38 chr12: 24,537,362-25,205,348 , GRCh37.p13 chr12: 24,690,296-25,358,282 , DAD1P1, 16 more genes
    nsv4842698copy number variation1nstd200human GRCh37 chr12: 24,844,677-25,298,755 , GRCh38.p12 chr12: 24,691,743-25,145,821 , LINC02909, 10 more genes
    nsv4729730copy number variation1nstd102humanPathogenic GRCh37 chr12: 21,582,333-24,920,271 , GRCh38.p12 chr12: 21,429,399-24,767,337 CMAS, ETNK1-DT, 34 more genes
    nsv4709830copy number variation1nstd195human GRCh37 chr12: 24,806,851-25,316,201 , GRCh38.p12 chr12: 24,653,917-25,163,267 , RN7SL38P, 10 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4578602copy number variation1nstd102humanPathogenic GRCh37 chr12: 23,457,173-25,177,321 , GRCh38.p12 chr12: 23,304,239-25,024,387 LOC105369697, RPL21P102, 13 more genes
    nsv4578254copy number variation1nstd102humanPathogenic GRCh37 chr12: 22,602,778-25,225,668 , GRCh38.p12 chr12: 22,449,844-25,072,734 DAD1P1, RPL21P102, 22 more genes
    nsv4457015copy number variation1nstd102humanUncertain significance GRCh37 chr12: 24,692,382-25,353,945 , GRCh38.p12 chr12: 24,539,448-25,201,011 LINC00477, RPL21P102, 14 more genes
    nsv4456793copy number variation1nstd102humanPathogenic GRCh37 chr12: 16,141,429-27,733,325 , GRCh38.p12 chr12: 15,988,495-27,580,392 PDE3A, ETFRF1, 133 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4387317copy number variation1nstd173human GRCh37 chr12: 24,686,646-25,353,987 , GRCh38.p12 chr12: 24,533,712-25,201,053 , DAD1P1, 15 more genes
    nsv4201623copy number variation1nstd166human GRCh37.p13 chr12: 24,229,749-24,988,958 , GRCh38.p12 chr12: 24,076,815-24,836,024 RPL21P102, LINC00477, 8 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 ENO2, SLC6A13, 684 more genes
    nsv3921202copy number variation1nstd102humanLikely benign NCBI36 chr12: 24,557,748-24,843,280 , GRCh37 chr12: 24,666,481-24,952,013 , GRCh38 chr12: 24,513,547-24,799,079 SOX5, KNOP1P1, 4 more genes
    nsv3918996copy number variation1nstd102humanLikely pathogenic NCBI36 chr12: 19,309,535-25,526,790 , GRCh37 chr12: 19,418,268-25,635,523 , GRCh38 chr12: 19,265,334-25,482,589 BCAT1, GYS2, 79 more genes
    nsv3918991copy number variation1nstd102humanUncertain significance GRCh37 chr12: 24,705,151-25,346,677 , GRCh38 chr12: 24,552,217-25,193,743 , NCBI36 chr12: 24,596,418-25,237,944 DAD1P1, LOC105369698, 14 more genes
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