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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097550copy number variation1nstd102humanUncertain significance GRCh37 chr5: 86,564,269-86,649,072 , GRCh38.p12 chr5: 87,268,452-87,353,255 RN7SL629P, CCNH, 3 more genes
    nsv7097549copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 86,564,269-86,564,827 , GRCh38.p12 chr5: 87,268,452-87,269,010 RASA1
    nsv7093437delins1nstd102humanPathogenic GRCh37 chr5: 86,564,400-86,564,420 , GRCh38 chr5: 87,268,583-87,268,603 RASA1
    nsv7054901inversion1nstd229human GRCh38 chr5: 86,506,255-87,299,369 , GRCh37.p13 chr5: 85,802,072-86,595,186 RN7SL629P, MIR4280, 12 more genes
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv7050687inversion1nstd229human GRCh38 chr5: 86,603,498-87,299,362 , GRCh37.p13 chr5: 85,899,315-86,595,179 RPL10AP9, LINC01949, 12 more genes
    nsv6775793copy number variation1nstd229human GRCh38 chr5: 87,250,201-87,273,600 , GRCh37.p13 chr5: 86,546,018-86,569,417 RASA1
    nsv6775704copy number variation1nstd229human GRCh38 chr5: 87,273,270-87,282,743 , GRCh37.p13 chr5: 86,569,087-86,578,560 RASA1
    nsv6775203copy number variation1nstd229human GRCh38 chr5: 87,341,838-87,344,594 , GRCh37.p13 chr5: 86,637,655-86,640,411 CCNH, RASA1
    nsv6772702copy number variation1nstd229human GRCh38 chr5: 87,318,827-87,323,223 , GRCh37.p13 chr5: 86,614,644-86,619,040 CCNH, LOC644285, 1 more genes
    nsv6772176copy number variation1nstd229human GRCh38 chr5: 87,293,984-87,315,864 , GRCh37.p13 chr5: 86,589,801-86,611,681 RASA1, RNU6-606P, 2 more genes
    nsv6769312copy number variation1nstd229human GRCh38 chr5: 87,377,495-87,489,205 , GRCh37.p13 chr5: 86,673,312-86,785,022 CCNH, LOC105379066, 2 more genes
    nsv6768539copy number variation1nstd229human GRCh38 chr5: 87,289,848-87,289,952 , GRCh37.p13 chr5: 86,585,665-86,585,769 RASA1
    nsv6766783copy number variation1nstd229human GRCh38 chr5: 87,323,934-87,327,353 , GRCh37.p13 chr5: 86,619,751-86,623,170 CCNH, LOC644285, 1 more genes
    nsv6766755copy number variation1nstd229human GRCh38 chr5: 87,314,204-87,315,471 , GRCh37.p13 chr5: 86,610,021-86,611,288 CCNH, RASA1
    nsv6762944copy number variation1nstd229human GRCh38 chr5: 87,046,508-87,930,460 , GRCh37.p13 chr5: 86,342,325-87,226,277 LINC02488, LOC105379065, 13 more genes
    nsv6761146copy number variation1nstd229human GRCh38 chr5: 87,281,259-87,283,448 , GRCh37.p13 chr5: 86,577,076-86,579,265 RASA1
    nsv6760436copy number variation1nstd229human GRCh38 chr5: 87,314,022-87,326,508 , GRCh37.p13 chr5: 86,609,839-86,622,325 CCNH, RASA1, 1 more genes
    nsv6760142copy number variation1nstd229human GRCh38 chr5: 87,250,795-87,267,778 , GRCh37.p13 chr5: 86,546,612-86,563,595 RASA1
    nsv6760025copy number variation1nstd229human GRCh38 chr5: 86,980,801-87,434,400 , GRCh37.p13 chr5: 86,276,618-86,730,217 LOC105379065, RN7SL629P, 11 more genes
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