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  • The following terms were not found in dbVar: Phenyl, dihydro, isoindole.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3121597copy number variation1nstd151human GRCh37 chr2: 113,671,366-113,675,359 , GRCh38.p12 chr2: 112,913,789-112,917,782 IL37
    nsv3137203copy number variation3nstd151human GRCh37 chr2: 113,671,366-113,674,830 , GRCh38.p12 chr2: 112,913,789-112,917,253 IL37
    nsv3127178copy number variation1nstd151human GRCh37 chr2: 113,670,587-113,672,841 , GRCh38.p12 chr2: 112,913,010-112,915,264 IL37
    nsv3137149copy number variation13nstd151human GRCh37 chr2: 234,526,351-234,527,213 , GRCh38.p12 chr2: 233,617,705-233,618,567 UGT1A8, UGT1A
    nsv3120030copy number variation1nstd151human GRCh37 chr2: 234,580,578-234,591,443 , GRCh38.p12 chr2: 233,671,932-233,682,797 UGT1A8, UGT1A9, 3 more genes
    esv3828609copy number variation237estd219human GRCh37 chr2: 234,542,941-234,545,367 , GRCh38.p12 chr2: 233,634,295-233,636,721 UGT1A, UGT1A10, 1 more genes
    esv3594678copy number variation237estd214human GRCh37 chr2: 234,542,941-234,545,367 , GRCh38.p12 chr2: 233,634,295-233,636,721 UGT1A, UGT1A10, 1 more genes
    nsv3138070copy number variation1nstd151human GRCh37 chr2: 113,593,140-113,671,436 , GRCh38.p12 chr2: 112,835,563-112,913,859 IL1B, XIAPP3, 2 more genes
    nsv3138266copy number variation1nstd151human GRCh37 chr2: 113,593,757-113,671,436 , GRCh38.p12 chr2: 112,836,180-112,913,859 IL37, LOC105373563, 2 more genes
    nsv3135234copy number variation2nstd151human GRCh37 chr2: 234,526,351-234,546,028 , GRCh38.p12 chr2: 233,617,705-233,637,382 UGT1A, UGT1A10, 1 more genes
    nsv3120178copy number variation1nstd151human GRCh37 chr2: 234,621,635-234,628,338 , GRCh38.p12 chr2: 233,712,989-233,719,692 UGT1A, UGT1A10, 7 more genes
    nsv3132515copy number variation1nstd151human GRCh37 chr2: 234,621,635-234,622,509 , GRCh38.p12 chr2: 233,712,989-233,713,863 UGT1A, UGT1A10, 5 more genes
    nsv3137773copy number variation1nstd151human GRCh37 chr2: 234,580,578-234,652,565 , GRCh38.p12 chr2: 233,671,932-233,743,919 UGT1A7, UGT1A9, 9 more genes
    nsv3123014copy number variation2nstd151human GRCh37 chr2: 234,580,578-234,638,644 , GRCh38.p12 chr2: 233,671,932-233,729,998 UGT1A, UGT1A6, 8 more genes
    nsv3122735copy number variation2nstd151human GRCh37 chr2: 234,637,770-234,652,565 , GRCh38.p12 chr2: 233,729,124-233,743,919 UGT1A7, UGT1A4, 8 more genes
    nsv3125001copy number variation1nstd151human GRCh37 chr2: 234,675,677-234,681,210 , GRCh38.p12 chr2: 233,767,031-233,772,564 UGT1A, UGT1A10, 9 more genes
    esv3828610copy number variation1estd219human GRCh37 chr2: 234,629,365-234,644,071 , GRCh38.p12 chr2: 233,720,719-233,735,425 UGT1A8, UGT1A5, 8 more genes
    esv3594679copy number variation1estd214human GRCh37 chr2: 234,629,365-234,644,071 , GRCh38.p12 chr2: 233,720,719-233,735,425 UGT1A8, UGT1A5, 8 more genes
    esv3828613copy number variation12estd219human GRCh37 chr2: 234,652,289-234,666,110 , GRCh38.p12 chr2: 233,743,643-233,757,464 UGT1A2P, UGT1A4, 10 more genes
    esv3594682copy number variation12estd214human GRCh37 chr2: 234,652,289-234,666,110 , GRCh38.p12 chr2: 233,743,643-233,757,464 UGT1A8, UGT1A5, 10 more genes
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