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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7042796inversion1nstd229human GRCh38 chr5: 134,802,336-135,650,849 , GRCh37.p13 chr5: 134,138,026-134,986,538 TXNDC15, LINC02900, 20 more genes
    nsv6796947copy number variation1nstd229human GRCh38 chr5: 134,864,817-134,887,328 , GRCh37.p13 chr5: 134,200,507-134,223,018 TXNDC15
    nsv6793697copy number variation1nstd229human GRCh38 chr5: 134,630,701-134,944,000 , GRCh37.p13 chr5: 133,966,391-134,279,690 SAR1B, MTCYBP18, 14 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
    nsv6786833copy number variation1nstd229human GRCh38 chr5: 134,886,091-134,886,118 , GRCh37.p13 chr5: 134,221,781-134,221,808 TXNDC15
    nsv6780128copy number variation1nstd229human GRCh38 chr5: 134,610,201-134,929,900 , GRCh37.p13 chr5: 133,945,891-134,265,590 MTCYBP18, RNU6-1311P, 14 more genes
    nsv6779962copy number variation1nstd229human GRCh38 chr5: 133,899,701-135,093,800 , GRCh37.p13 chr5: 133,235,392-134,429,490 TXNDC15, PPP2CA, 37 more genes
    nsv6779172copy number variation1nstd229human GRCh38 chr5: 134,710,279-135,016,247 , GRCh37.p13 chr5: 134,045,969-134,351,937 MTND5P11, RPL34P13, 12 more genes
    nsv6557718inversion1nstd223human GRCh38 chr5: 134,883,836-134,884,433 , GRCh37.p13 chr5: 134,219,526-134,220,123 TXNDC15
    nsv6412678copy number variation1nstd223human GRCh38 chr5: 134,885,119-134,887,360 , GRCh37.p13 chr5: 134,220,809-134,223,050 TXNDC15
    nsv6399574copy number variation1nstd223human GRCh38 chr5: 134,888,954-134,889,293 , GRCh37.p13 chr5: 134,224,644-134,224,983 TXNDC15
    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
    nsv6296246copy number variation1nstd186human GRCh37 chr5: 134,220,855-134,223,010 , GRCh38.p12 chr5: 134,885,165-134,887,320 TXNDC15
    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
    nsv6007993copy number variation1nstd212human GRCh38 chr5: 134,883,983-134,884,086 , GRCh37.p13 chr5: 134,219,673-134,219,776 TXNDC15
    nsv5679839mobile element insertion2nstd211human GRCh38 chr5: 134,895,682-134,895,682 , GRCh37.p13 chr5: 134,231,372-134,231,372 TXNDC15
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