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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042796inversion1nstd229human GRCh38 chr5: 134,802,336-135,650,849 , GRCh37.p13 chr5: 134,138,026-134,986,538 TXNDC15, LINC02900, 20 more genes
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6636280copy number variation1nstd102humanUncertain significance GRCh37 chr5: 134,524,754-135,283,222 , GRCh38.p12 chr5: 135,189,064-135,947,533 LINC02900, DCANP1, 12 more genes
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6313506copy number variation1nstd102humanUncertain significance GRCh37 chr5: 132,829,317-134,983,855 , GRCh38.p12 chr5: 133,493,625-135,648,166 RPS10P11, PCBD2, 47 more genes
    nsv6135646copy number variation1nstd213human GRCh37 chr5: 124,370,000-136,400,001 , GRCh38.p12 chr5: 125,034,307-137,064,312 ACTBP4, ALDH7A1, 181 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135114copy number variation1nstd213human GRCh37 chr5: 133,550,000-135,990,001 , GRCh38.p12 chr5: 134,214,309-136,654,312 CAMLG, IL9, 53 more genes
    nsv5038943inversion1nstd200human GRCh38 chr5: 135,468,456-136,310,303 , GRCh37.p13 chr5: 134,804,146-135,645,991 SMAD5, SMAD5-AS1, 15 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3920627copy number variation1nstd102humanPathogenic NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694 MIR1289-2, DCANP1, 138 more genes
    nsv3919979copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626 FBXL21P, MIR5692C1, 92 more genes
    nsv3916850copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,962,196-135,150,743 , NCBI36 chr5: 130,990,095-135,178,642 , GRCh38 chr5: 131,626,503-135,815,054 SLC25A48-AS1, CTB-3M24.3, 96 more genes
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