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Items: 1 to 20 of 126

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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
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7044511inversion1nstd229human GRCh38 chr5: 134,400,640-134,406,142 , GRCh37.p13 chr5: 133,736,331-133,741,833 CDKN2AIPNL
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv6796311copy number variation1nstd229human GRCh38 chr5: 134,406,655-134,407,536 , GRCh37.p13 chr5: 133,742,346-133,743,227 CDKN2AIPNL
    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
    nsv6785601copy number variation1nstd229human GRCh38 chr5: 134,391,534-134,462,766 , GRCh37.p13 chr5: 133,727,225-133,798,457 LINC02999, CDKN2AIPNL, 2 more genes
    nsv6783810copy number variation1nstd229human GRCh38 chr5: 134,398,603-134,401,370 , GRCh37.p13 chr5: 133,734,294-133,737,061 CDKN2AIPNL
    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
    nsv6559579inversion1nstd223human GRCh38 chr5: 134,399,738-134,400,782 , GRCh37.p13 chr5: 133,735,429-133,736,473 CDKN2AIPNL
    nsv6558117inversion1nstd223human GRCh38 chr5: 134,395,285-134,401,014 , GRCh37.p13 chr5: 133,730,976-133,736,705 CDKN2AIPNL
    nsv6399885copy number variation1nstd223human GRCh38 chr5: 134,406,612-134,407,533 , GRCh37.p13 chr5: 133,742,303-133,743,224 CDKN2AIPNL
    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
    nsv5466659copy number variation1nstd206human GRCh38 chr5: 134,406,640-134,407,554 , GRCh37.p13 chr5: 133,742,331-133,743,245 CDKN2AIPNL
    nsv5300642copy number variation1nstd204human GRCh38.p13 chr5: 134,406,630-134,407,563 , GRCh37.p13 chr5: 133,742,321-133,743,254 CDKN2AIPNL
    nsv5090718mobile element insertion1nstd203human GRCh38 chr5: 134,403,488-134,403,503 , GRCh37.p13 chr5: 133,739,179-133,739,194 CDKN2AIPNL
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