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Items: 1 to 20 of 610

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7098684copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,573,453-103,575,949 , GRCh37.p13 chr14: 103,039,790-104,042,286 MARK3, GCSHP2, 34 more genes
    nsv7094241copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,442,029-105,861,009 , GRCh38.p12 chr14: 101,975,692-105,394,672 LOC107984670, MARK3, 101 more genes
    nsv7094007copy number variation1nstd102humanUncertain significance GRCh37 chr14: 102,228,231-105,861,009 , GRCh38.p12 chr14: 101,761,894-105,394,672 CLBA1, BAG5, 105 more genes
    nsv6977159copy number variation1nstd229human GRCh38 chr14: 103,393,897-103,396,743 , GRCh37.p13 chr14: 103,860,234-103,863,080 MARK3
    nsv6977149copy number variation1nstd229human GRCh38 chr14: 102,678,201-103,458,700 , GRCh37.p13 chr14: 103,144,538-103,925,037 LBHD2, LOC105370686, 25 more genes
    nsv6976511copy number variation1nstd229human GRCh38 chr14: 103,416,401-103,419,200 , GRCh37.p13 chr14: 103,882,738-103,885,537 MARK3
    nsv6975759copy number variation1nstd229human GRCh38 chr14: 103,094,284-103,544,082 , GRCh37.p13 chr14: 103,560,621-104,010,419 LINC00605, EIF5-DT, 21 more genes
    nsv6975093copy number variation1nstd229human GRCh38 chr14: 103,393,898-103,397,264 , GRCh37.p13 chr14: 103,860,235-103,863,601 MARK3
    nsv6972428copy number variation1nstd229human GRCh38 chr14: 103,480,939-103,483,826 , GRCh37.p13 chr14: 103,947,276-103,950,163 MARK3
    nsv6970464copy number variation1nstd229human GRCh38 chr14: 103,388,567-103,402,705 , GRCh37.p13 chr14: 103,854,904-103,869,042 MARK3
    nsv6969606copy number variation1nstd229human GRCh38 chr14: 103,038,255-103,449,234 , GRCh37.p13 chr14: 103,504,592-103,915,571 GCSHP2, LOC105370685, 21 more genes
    nsv6967048copy number variation1nstd229human GRCh38 chr14: 103,461,701-103,827,300 , GRCh37.p13 chr14: 103,928,038-104,293,637 COA8, XRCC3, 12 more genes
    nsv6966907copy number variation1nstd229human GRCh38 chr14: 103,341,601-103,757,500 , GRCh37.p13 chr14: 103,807,938-104,223,837 TRMT61A, RNU7-160P, 16 more genes
    nsv6965912copy number variation1nstd229human GRCh38 chr14: 103,476,764-103,476,803 , GRCh37.p13 chr14: 103,943,101-103,943,140 MARK3
    nsv6964500copy number variation1nstd229human GRCh38 chr14: 103,414,578-103,418,896 , GRCh37.p13 chr14: 103,880,915-103,885,233 MARK3
    nsv6964075copy number variation1nstd229human GRCh38 chr14: 103,419,869-103,427,741 , GRCh37.p13 chr14: 103,886,206-103,894,078 MARK3
    nsv6959257copy number variation1nstd229human GRCh38 chr14: 103,378,375-103,401,335 , GRCh37.p13 chr14: 103,844,712-103,867,672 MARK3
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
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