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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054553inversion1nstd229human GRCh38 chr4: 82,859,414-82,862,998 , GRCh37.p13 chr4: 83,780,567-83,784,151 SEC31A
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv6755635copy number variation1nstd229human GRCh38 chr4: 82,842,812-82,848,831 , GRCh37.p13 chr4: 83,763,965-83,769,984 SEC31A
    nsv6753525copy number variation1nstd229human GRCh38 chr4: 82,887,701-82,890,300 , GRCh37.p13 chr4: 83,808,854-83,811,453 SEC31A
    nsv6752757copy number variation1nstd229human GRCh38 chr4: 82,884,189-82,888,486 , GRCh37.p13 chr4: 83,805,342-83,809,639 SEC31A
    nsv6750199copy number variation1nstd229human GRCh38 chr4: 82,893,394-82,898,066 , GRCh37.p13 chr4: 83,814,547-83,819,219 THAP9-AS1, SEC31A, 2 more genes
    nsv6748801copy number variation1nstd229human GRCh38 chr4: 82,837,378-82,841,496 , GRCh37.p13 chr4: 83,758,531-83,762,649 SEC31A
    nsv6747654copy number variation1nstd229human GRCh38 chr4: 82,885,334-82,888,713 , GRCh37.p13 chr4: 83,806,487-83,809,866 SEC31A
    nsv6746022copy number variation1nstd229human GRCh38 chr4: 82,837,759-82,837,952 , GRCh37.p13 chr4: 83,758,912-83,759,105 SEC31A
    nsv6745597copy number variation1nstd229human GRCh38 chr4: 82,842,480-82,848,802 , GRCh37.p13 chr4: 83,763,633-83,769,955 SEC31A
    nsv6742138copy number variation1nstd229human GRCh38 chr4: 82,533,814-82,964,129 , GRCh37.p13 chr4: 83,454,967-83,885,282 THAP9, MIR575, 10 more genes
    nsv6741240copy number variation1nstd229human GRCh38 chr4: 82,673,201-82,885,000 , GRCh37.p13 chr4: 83,594,354-83,806,153 MIR575, SLC66A2P2, 2 more genes
    nsv6738569copy number variation1nstd229human GRCh38 chr4: 82,836,139-82,841,189 , GRCh37.p13 chr4: 83,757,292-83,762,342 SEC31A
    nsv6575408inversion1nstd223human GRCh38 chr4: 82,871,683-82,871,860 , GRCh37.p13 chr4: 83,792,836-83,793,013 SEC31A
    nsv6571133inversion1nstd223human GRCh38 chr4: 82,819,968-82,821,272 , GRCh37.p13 chr4: 83,741,121-83,742,425 SEC31A
    nsv6566027inversion1nstd223human GRCh38 chr4: 82,858,300-82,858,553 , GRCh37.p13 chr4: 83,779,453-83,779,706 SEC31A
    nsv6565691inversion1nstd223human GRCh38 chr4: 82,883,826-82,884,272 , GRCh37.p13 chr4: 83,804,979-83,805,425 SEC31A
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
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