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Items: 1 to 20 of 733

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137007copy number variation1nstd102humanPathogenic GRCh38 chr9: 14,762,351-14,792,870 , GRCh37.p13 chr9: 14,762,349-14,792,868 FREM1, LOC105375979
    nsv7098444copy number variation1nstd102humanPathogenic GRCh37 chr9: 14,801,630-14,859,502 , GRCh38.p12 chr9: 14,801,632-14,859,504 FREM1, RNU6-1260P
    nsv7097712copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 14,737,394-14,868,975 , GRCh38.p12 chr9: 14,737,396-14,868,977 LOC105375979, FREM1, 1 more genes
    nsv7077739inversion1nstd229human GRCh38 chr9: 14,879,914-14,889,742 , GRCh37.p13 chr9: 14,879,912-14,889,740 FREM1
    nsv7074147inversion1nstd229human GRCh38 chr9: 14,880,074-14,886,773 , GRCh37.p13 chr9: 14,880,072-14,886,771 FREM1
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7072115inversion1nstd229human GRCh38 chr9: 12,276,809-15,153,662 , GRCh37.p13 chr9: 12,276,809-15,153,660 PES1P2, RNU6-559P, 30 more genes
    nsv7071502inversion1nstd229human GRCh38 chr9: 14,854,361-15,041,098 , GRCh37.p13 chr9: 14,854,359-15,041,096 FREM1, LOC105375980, 3 more genes
    nsv7071345inversion1nstd229human GRCh38 chr9: 14,900,646-14,960,849 , GRCh37.p13 chr9: 14,900,644-14,960,847 FREM1, LDHAP4
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062657inversion1nstd229human GRCh38 chr9: 14,747,611-14,747,643 , GRCh37.p13 chr9: 14,747,609-14,747,641 FREM1
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv7058778inversion1nstd229human GRCh38 chr9: 14,730,744-14,731,543 , GRCh37.p13 chr9: 14,730,742-14,731,541 FREM1
    nsv7058270inversion1nstd229human GRCh38 chr9: 14,773,608-14,773,682 , GRCh37.p13 chr9: 14,773,606-14,773,680 FREM1
    nsv6877622copy number variation1nstd229human GRCh38 chr9: 14,226,508-15,063,519 , GRCh37.p13 chr9: 14,226,507-15,063,517 LDHAP4, CDCA4P1, 11 more genes
    nsv6875930copy number variation1nstd229human GRCh38 chr9: 14,874,701-14,877,700 , GRCh37.p13 chr9: 14,874,699-14,877,698 FREM1
    nsv6875529copy number variation1nstd229human GRCh38 chr9: 14,889,211-14,907,810 , GRCh37.p13 chr9: 14,889,209-14,907,808 FREM1
    nsv6875053copy number variation1nstd229human GRCh38 chr9: 14,868,219-14,891,950 , GRCh37.p13 chr9: 14,868,217-14,891,948 FREM1
    nsv6872982copy number variation1nstd229human GRCh38 chr9: 14,866,155-15,106,564 , GRCh37.p13 chr9: 14,866,153-15,106,562 LDHAP4, LOC389705, 4 more genes
    nsv6872841copy number variation1nstd229human GRCh38 chr9: 14,627,573-14,801,777 , GRCh37.p13 chr9: 14,627,571-14,801,775 CER1, FREM1, 2 more genes
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