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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv6994145copy number variation1nstd229human GRCh38 chr16: 19,849,701-19,854,752 , GRCh37.p13 chr16: 19,861,023-19,866,074 IQCK, GPRC5B
    nsv6988648copy number variation1nstd229human GRCh38 chr16: 19,880,915-19,888,333 , GRCh37.p13 chr16: 19,892,237-19,899,655 GPRC5B
    nsv6980834copy number variation1nstd229human GRCh38 chr16: 19,886,212-19,897,370 , GRCh37.p13 chr16: 19,897,534-19,908,692 GPRC5B
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6589702inversion1nstd223human GRCh38 chr16: 19,877,928-19,878,331 , GRCh37.p13 chr16: 19,889,250-19,889,653 GPRC5B
    nsv6513609copy number variation1nstd223human GRCh38 chr16: 19,868,046-19,869,081 , GRCh37.p13 chr16: 19,879,368-19,880,403 GPRC5B
    nsv6506360copy number variation1nstd223human GRCh38 chr16: 19,868,201-19,869,100 , GRCh37.p13 chr16: 19,879,523-19,880,422 GPRC5B
    nsv6498312copy number variation1nstd223human GRCh38 chr16: 19,886,212-19,897,370 , GRCh37.p13 chr16: 19,897,534-19,908,692 GPRC5B
    nsv6133261copy number variation1nstd213human GRCh37 chr16: 19,140,000-21,360,001 , GRCh38.p12 chr16: 19,128,678-21,348,680 CRYM, GP2, 49 more genes
    nsv6133258copy number variation1nstd213human GRCh37 chr16: 16,530,000-21,500,001 , GRCh38.p12 chr16: 16,436,143-21,488,680 CRYM, GP2, 93 more genes
    nsv6133165copy number variation1nstd213human GRCh37 chr16: 19,775,049-19,907,841 , GRCh38.p12 chr16: 19,763,727-19,896,519 GPRC5B, IQCK, 2 more genes
    nsv6133013copy number variation1nstd213human GRCh37 chr16: 19,620,000-22,460,001 , GRCh38.p12 chr16: 19,608,678-22,448,680 CDR2, CRYM, 76 more genes
    nsv5977368insertion1nstd209human GRCh38 chr16: 19,879,275-19,879,275 , GRCh37.p13 chr16: 19,890,597-19,890,597 GPRC5B
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5533026copy number variation1nstd206human GRCh38 chr16: 19,862,747-19,867,910 , GRCh37.p13 chr16: 19,874,069-19,879,232 GPRC5B
    nsv5145910mobile element insertion1nstd203human GRCh38 chr16: 19,860,433-19,860,448 , GRCh37.p13 chr16: 19,871,755-19,871,770 GPRC5B
    nsv5003077copy number variation1nstd200human GRCh38 chr16: 19,863,107-19,863,182 , GRCh37.p13 chr16: 19,874,429-19,874,504 GPRC5B
    nsv4994526copy number variation1nstd200human GRCh38 chr16: 19,886,212-19,897,370 , GRCh37.p13 chr16: 19,897,534-19,908,692 GPRC5B
    nsv4850652copy number variation1nstd200human GRCh37 chr16: 19,874,429-19,874,504 , GRCh38.p12 chr16: 19,863,107-19,863,182 GPRC5B
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