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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071358inversion1nstd229human GRCh38 chr21: 23,691,748-31,155,798 , GRCh37.p13 chr21: 25,064,065-32,528,116 LLPHP2, KRTAP20-3, 126 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
    nsv7066036inversion1nstd229human GRCh38 chr21: 29,840,839-33,329,795 , GRCh37.p13 chr21: 31,213,156-34,702,101 SYNJ1, CLDN8, 95 more genes
    nsv7065590inversion1nstd229human GRCh38 chr21: 23,756,613-30,931,318 , GRCh37.p13 chr21: 25,128,930-32,303,637 LINC01697, LOC105372753, 119 more genes
    nsv7028081copy number variation1nstd229human GRCh38 chr21: 30,255,704-30,287,359 , GRCh37.p13 chr21: 31,628,022-31,659,677 RPL8P2, KRTAP24-1, 1 more genes
    nsv7023945copy number variation1nstd229human GRCh38 chr21: 27,856,301-31,095,924 , GRCh37.p13 chr21: 29,228,620-32,468,242 KRTAP19-11P, KRTAP6-2, 78 more genes
    nsv7022660copy number variation1nstd229human GRCh38 chr21: 30,110,165-30,738,109 , GRCh37.p13 chr21: 31,482,483-32,110,427 LOC105372773, KRTAP13-5P, 37 more genes
    nsv6637957copy number variation1nstd102humanUncertain significance GRCh37 chr21: 30,909,762-32,182,012 , GRCh38.p12 chr21: 29,537,441-30,809,694 CLDN8, KRTAP8-2P, 46 more genes
    nsv6637343copy number variation1nstd102humanUncertain significance GRCh37 chr21: 29,243,314-32,472,073 , GRCh38.p12 chr21: 27,870,995-31,099,755 GAPDHP14, LINC00189, 78 more genes
    nsv6627149copy number variation1nstd224human GRCh37 chr21: 31,587,597-31,720,788 , GRCh38.p12 chr21: 30,215,279-30,348,470 CLDN8, KRTAP23-1, 5 more genes
    nsv6627000copy number variation1nstd224human GRCh37 chr21: 31,176,283-31,687,009 , GRCh38.p12 chr21: 29,803,966-30,314,691 GRIK1, CLDN8, 5 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6596327inversion1nstd223human GRCh38 chr21: 28,377,391-35,730,332 , GRCh37.p13 chr21: 29,749,712-37,102,630 , LOC107985515, 161 more genes
    nsv6546600copy number variation1nstd223human GRCh38 chr21: 29,796,823-30,635,785 , GRCh37.p13 chr21: 31,169,140-32,008,104 KRTAP26-1, KRTAP20-1, 35 more genes
    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
    nsv6314196copy number variation1nstd102humanUncertain significance GRCh37 chr21: 27,185,913-35,853,445 , GRCh38.p12 chr21: 25,813,602-34,481,147 RPL12P9, CLDN17, 173 more genes
    nsv6313951copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,041,209-48,097,372 , GRCh38.p12 chr21: 13,668,888-46,677,460 LOC107985515, ATP5PF, 606 more genes
    nsv6291702copy number variation1nstd102humanUncertain significance GRCh37 chr21: 31,171,624-31,891,623 , GRCh38.p12 chr21: 29,799,307-30,519,305 KRTAP15-1, KRTAP13-5P, 24 more genes
    nsv6291618copy number variation1nstd102humanUncertain significance GRCh37 chr21: 31,119,490-32,485,971 , GRCh38.p12 chr21: 29,747,171-31,113,653 KRTAP19-1, LOC105372772, 52 more genes
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