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Items: 1 to 20 of 1554

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145620copy number variation1nstd232human GRCh37.p13 chr5: 132,657,941-132,657,992 , GRCh38.p12 chr5: 133,322,249-133,322,300 FSTL4
    nsv7139841copy number variation1nstd232human GRCh37.p13 chr5: 132,657,955-132,658,004 , GRCh38.p12 chr5: 133,322,263-133,322,312 FSTL4
    nsv7137951insertion1nstd232human GRCh37.p13 chr5: 132,961,438-132,961,438 , GRCh38.p12 chr5: 133,625,747-133,625,747 FSTL4
    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
    nsv7053035inversion1nstd229human GRCh38 chr5: 133,341,287-133,352,435 , GRCh37.p13 chr5: 132,676,979-132,688,127 FSTL4
    nsv7052006inversion1nstd229human GRCh38 chr5: 133,706,074-133,706,174 , GRCh37.p13 chr5: 133,041,765-133,041,865 FSTL4
    nsv7051542inversion1nstd229human GRCh38 chr5: 133,748,527-133,748,574 , GRCh37.p13 chr5: 133,084,218-133,084,265 FSTL4
    nsv7051034inversion1nstd229human GRCh38 chr5: 133,683,568-133,683,680 , GRCh37.p13 chr5: 133,019,259-133,019,371 FSTL4
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7049693inversion1nstd229human GRCh38 chr5: 133,349,077-133,349,156 , GRCh37.p13 chr5: 132,684,769-132,684,848 FSTL4
    nsv7047603inversion1nstd229human GRCh38 chr5: 133,629,500-133,636,106 , GRCh37.p13 chr5: 132,965,191-132,971,797 FSTL4
    nsv7044423inversion1nstd229human GRCh38 chr5: 133,315,672-133,320,356 , GRCh37.p13 chr5: 132,651,364-132,656,048 FSTL4
    nsv7043160inversion1nstd229human GRCh38 chr5: 133,315,070-133,320,361 , GRCh37.p13 chr5: 132,650,762-132,656,053 FSTL4
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv7040381inversion1nstd229human GRCh38 chr5: 133,347,698-133,352,435 , GRCh37.p13 chr5: 132,683,390-132,688,127 FSTL4
    nsv6797136copy number variation1nstd229human GRCh38 chr5: 133,590,657-133,601,229 , GRCh37.p13 chr5: 132,926,348-132,936,920 FSTL4
    nsv6797065copy number variation1nstd229human GRCh38 chr5: 133,691,306-133,698,110 , GRCh37.p13 chr5: 133,026,997-133,033,801 FSTL4
    nsv6796981copy number variation1nstd229human GRCh38 chr5: 133,742,113-133,744,759 , GRCh37.p13 chr5: 133,077,804-133,080,450 FSTL4
    nsv6796721copy number variation1nstd229human GRCh38 chr5: 133,387,678-133,402,521 , GRCh37.p13 chr5: 132,723,370-132,738,213 CTB-3M24.3, FSTL4
    nsv6796519copy number variation1nstd229human GRCh38 chr5: 133,215,147-133,216,527 , GRCh37.p13 chr5: 132,550,839-132,552,219 CTB-49A3.2, FSTL4
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