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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141819insertion1nstd232human GRCh37.p13 chr21: 34,625,135-34,625,135 , GRCh38.p12 chr21: 33,252,830-33,252,830 IFNAR2
    nsv7096093copy number variation1nstd102humanPathogenic GRCh37 chr21: 34,614,228-34,635,805 , GRCh38.p12 chr21: 33,241,923-33,263,500 IFNAR2
    nsv7095918copy number variation1nstd102humanPathogenic GRCh37 chr21: 34,614,228-34,614,302 , GRCh38.p12 chr21: 33,241,923-33,241,997 IFNAR2
    nsv7075861inversion1nstd229human GRCh38 chr21: 32,596,447-36,013,453 , GRCh37.p13 chr21: 33,968,757-37,385,751 , IFNAR2, 64 more genes
    nsv7070554inversion1nstd229human GRCh38 chr21: 28,138,154-35,660,050 , GRCh37.p13 chr21: 29,510,473-37,032,348 , OR7E23P, 160 more genes
    nsv7070253inversion1nstd229human GRCh38 chr21: 28,377,443-35,730,342 , GRCh37.p13 chr21: 29,749,764-37,102,640 , HUNK, 161 more genes
    nsv7070001inversion1nstd229human GRCh38 chr21: 33,261,086-33,279,270 , GRCh37.p13 chr21: 34,633,391-34,651,575 IL10RB, IL10RB-DT, 1 more genes
    nsv7066036inversion1nstd229human GRCh38 chr21: 29,840,839-33,329,795 , GRCh37.p13 chr21: 31,213,156-34,702,101 SYNJ1, CLDN8, 95 more genes
    nsv7036880copy number variation1nstd229human GRCh38 chr21: 33,235,725-33,240,188 , GRCh37.p13 chr21: 34,608,030-34,612,493 IFNAR2
    nsv7033148copy number variation1nstd229human GRCh38 chr21: 33,230,959-33,236,401 , GRCh37.p13 chr21: 34,603,264-34,608,706 IFNAR2
    nsv7030302copy number variation1nstd229human GRCh38 chr21: 33,231,426-33,231,481 , GRCh37.p13 chr21: 34,603,731-34,603,786 IFNAR2
    nsv7029350copy number variation1nstd229human GRCh38 chr21: 33,266,031-33,266,127 , GRCh37.p13 chr21: 34,638,336-34,638,432 IL10RB-DT, IL10RB, 1 more genes
    nsv7027470copy number variation1nstd229human GRCh38 chr21: 33,159,601-33,307,500 , GRCh37.p13 chr21: 34,531,907-34,679,805 IL10RB, LOC105372787, 3 more genes
    nsv6634422copy number variation1nstd102humanUncertain significance GRCh37 chr21: 33,032,083-34,809,269 , GRCh38.p12 chr21: 31,659,770-33,436,962 SOD1, CFAP298, 39 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6600020inversion1nstd223human GRCh38 chr21: 33,261,144-33,261,743 , GRCh37.p13 chr21: 34,633,449-34,634,048 IFNAR2
    nsv6599047inversion1nstd223human GRCh38 chr21: 33,261,205-33,261,713 , GRCh37.p13 chr21: 34,633,510-34,634,018 IFNAR2
    nsv6596327inversion1nstd223human GRCh38 chr21: 28,377,391-35,730,332 , GRCh37.p13 chr21: 29,749,712-37,102,630 , LOC107985515, 161 more genes
    nsv6536166copy number variation1nstd223human GRCh38 chr21: 33,235,725-33,240,186 , GRCh37.p13 chr21: 34,608,030-34,612,491 IFNAR2
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
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