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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,178,392-66,433,436 , GRCh38.p12 chr11: 66,410,921-66,665,965 MRPL11, NPAS4, 15 more genes
    nsv6917968copy number variation1nstd229human GRCh38 chr11: 66,648,756-66,650,807 , GRCh37.p13 chr11: 66,416,227-66,418,278 RBM4
    nsv6916455copy number variation1nstd229human GRCh38 chr11: 66,658,319-66,660,904 , GRCh37.p13 chr11: 66,425,790-66,428,375 RBM4
    nsv6914912copy number variation1nstd229human GRCh38 chr11: 66,643,888-66,643,922 , GRCh37.p13 chr11: 66,411,359-66,411,393 RBM4, RBM14-RBM4
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905609copy number variation1nstd229human GRCh38 chr11: 66,664,657-66,676,189 , GRCh37.p13 chr11: 66,432,128-66,443,660 RBM4B, RBM4
    nsv6898816copy number variation1nstd229human GRCh38 chr11: 66,649,201-66,650,961 , GRCh37.p13 chr11: 66,416,672-66,418,432 RBM4
    nsv6595062inversion1nstd223human GRCh38 chr11: 66,657,284-66,657,541 , GRCh37.p13 chr11: 66,424,755-66,425,012 RBM4
    nsv6473643copy number variation1nstd223human GRCh38 chr11: 66,649,128-66,653,467 , GRCh37.p13 chr11: 66,416,599-66,420,938 RBM4
    nsv6465745copy number variation1nstd223human GRCh38 chr11: 66,662,601-66,664,200 , GRCh37.p13 chr11: 66,430,072-66,431,671 RBM4, RBM4B
    nsv6458302copy number variation1nstd223human GRCh38 chr11: 66,651,401-66,653,453 , GRCh37.p13 chr11: 66,418,872-66,420,924 RBM4
    nsv6457071copy number variation1nstd223human GRCh38 chr11: 66,649,201-66,650,957 , GRCh37.p13 chr11: 66,416,672-66,418,428 RBM4
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132113copy number variation1nstd213human GRCh37 chr11: 66,380,000-66,540,001 , GRCh38.p12 chr11: 66,612,529-66,772,530 RBM14, RBM4B, 8 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5926137copy number variation1nstd209human GRCh38 chr11: 66,642,424-66,671,565 , GRCh37.p13 chr11: 66,409,895-66,439,036 RBM4, RBM4B, 1 more genes
    nsv5858208copy number variation1nstd209human GRCh38 chr11: 66,658,306-66,671,266 , GRCh37.p13 chr11: 66,425,777-66,438,737 RBM4B, RBM4
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