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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CSF2, LOC402229, 99 more genes
    nsv7055312inversion1nstd229human GRCh38 chr5: 134,007,166-134,301,352 , GRCh37.p13 chr5: 133,342,857-133,637,043 PPP2CA, TCF7, 5 more genes
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7044992inversion1nstd229human GRCh38 chr5: 134,017,332-134,301,206 , GRCh37.p13 chr5: 133,353,023-133,636,897 SKP1, VDAC1, 5 more genes
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv7040231inversion1nstd229human GRCh38 chr5: 134,017,287-134,301,206 , GRCh37.p13 chr5: 133,352,978-133,636,897 SKP1, VDAC1, 5 more genes
    nsv6797317copy number variation1nstd229human GRCh38 chr5: 134,208,584-134,208,624 , GRCh37.p13 chr5: 133,544,275-133,544,315 PPP2CA
    nsv6789730copy number variation1nstd229human GRCh38 chr5: 134,132,745-134,207,867 , GRCh37.p13 chr5: 133,468,436-133,543,558 SKP1, TCF7, 1 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
    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
    nsv6569546inversion1nstd223human GRCh38 chr5: 134,007,166-134,301,352 , GRCh37.p13 chr5: 133,342,857-133,637,043 PPP2CA, SKP1, 5 more genes
    nsv6565256inversion1nstd223human GRCh38 chr5: 134,198,331-134,198,766 , GRCh37.p13 chr5: 133,534,022-133,534,457 PPP2CA
    nsv6564539inversion1nstd223human GRCh38 chr5: 134,211,494-134,212,093 , GRCh37.p13 chr5: 133,547,185-133,547,784 PPP2CA
    nsv6562521inversion1nstd223human GRCh38 chr5: 134,192,894-134,193,629 , GRCh37.p13 chr5: 133,528,585-133,529,320 PPP2CA
    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
    nsv6068358insertion1nstd212human GRCh38 chr5: 134,212,448-134,212,448 , GRCh37.p13 chr5: 133,548,139-133,548,139 PPP2CA
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