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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096977copy number variation1nstd102humanPathogenic GRCh37 chr4: 123,818,759-124,235,219 , GRCh38.p12 chr4: 122,897,604-123,314,064 FGF2, COILP2, 2 more genes
    nsv7096974copy number variation1nstd102humanUncertain significance GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551 RN7SL335P, QRFPR, 40 more genes
    nsv7051830inversion1nstd229human GRCh38 chr4: 122,021,125-125,223,020 , GRCh37.p13 chr4: 122,942,280-126,144,175 SPRY1, ANKRD50, 29 more genes
    nsv7047579inversion1nstd229human GRCh38 chr4: 122,858,114-122,858,238 , GRCh37.p13 chr4: 123,779,269-123,779,393 FGF2
    nsv7046043inversion1nstd229human GRCh38 chr4: 121,571,489-125,148,298 , GRCh37.p13 chr4: 122,492,644-126,069,453 TRC-GCA2-1, LINC02435, 39 more genes
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv7040293inversion1nstd229human GRCh38 chr4: 122,406,938-123,167,062 , GRCh37.p13 chr4: 123,328,093-124,088,217 IL21-AS1, NUDT6, 11 more genes
    nsv6755628copy number variation1nstd229human GRCh38 chr4: 122,853,561-122,853,971 , GRCh37.p13 chr4: 123,774,716-123,775,126 FGF2
    nsv6754528copy number variation1nstd229human GRCh38 chr4: 122,606,959-123,206,244 , GRCh37.p13 chr4: 123,528,114-124,127,399 BBS12, RPS26P23, 9 more genes
    nsv6751566copy number variation1nstd229human GRCh38 chr4: 122,780,892-122,950,556 , GRCh37.p13 chr4: 123,702,047-123,871,711 FGF2, RPL34P12, 3 more genes
    nsv6747812copy number variation1nstd229human GRCh38 chr4: 122,863,201-122,883,400 , GRCh37.p13 chr4: 123,784,356-123,804,555 FGF2
    nsv6747181copy number variation1nstd229human GRCh38 chr4: 122,845,767-122,858,021 , GRCh37.p13 chr4: 123,766,922-123,779,176 FGF2
    nsv6746121copy number variation1nstd229human GRCh38 chr4: 122,893,239-122,898,785 , GRCh37.p13 chr4: 123,814,394-123,819,940 NUDT6, FGF2
    nsv6745747copy number variation1nstd229human GRCh38 chr4: 122,876,324-122,877,500 , GRCh37.p13 chr4: 123,797,479-123,798,655 FGF2
    nsv6743106copy number variation1nstd229human GRCh38 chr4: 122,853,084-122,863,293 , GRCh37.p13 chr4: 123,774,239-123,784,448 FGF2
    nsv6741312copy number variation1nstd229human GRCh38 chr4: 122,868,750-122,873,249 , GRCh37.p13 chr4: 123,789,905-123,794,404 FGF2
    nsv6741274copy number variation1nstd229human GRCh38 chr4: 122,884,759-122,884,801 , GRCh37.p13 chr4: 123,805,914-123,805,956 FGF2
    nsv6741241copy number variation1nstd229human GRCh38 chr4: 122,897,151-122,901,279 , GRCh37.p13 chr4: 123,818,306-123,822,434 NUDT6, FGF2
    nsv6741150copy number variation1nstd229human GRCh38 chr4: 122,890,801-122,895,400 , GRCh37.p13 chr4: 123,811,956-123,816,555 FGF2, NUDT6
    nsv6740278copy number variation1nstd229human GRCh38 chr4: 122,851,923-122,855,609 , GRCh37.p13 chr4: 123,773,078-123,776,764 FGF2
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