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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052793inversion1nstd229human GRCh38 chr6: 138,947,115-138,947,709 , GRCh37.p13 chr6: 139,268,252-139,268,846 REPS1
    nsv7051052inversion1nstd229human GRCh38 chr6: 138,979,260-138,979,295 , GRCh37.p13 chr6: 139,300,397-139,300,432 REPS1
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv7049872inversion1nstd229human GRCh38 chr6: 138,962,723-138,965,044 , GRCh37.p13 chr6: 139,283,860-139,286,181 REPS1
    nsv7048636inversion1nstd229human GRCh38 chr6: 138,740,942-138,941,272 , GRCh37.p13 chr6: 139,062,079-139,262,409 CCDC28A, LOC107986650, 4 more genes
    nsv7040858inversion1nstd229human GRCh38 chr6: 138,938,769-138,953,490 , GRCh37.p13 chr6: 139,259,906-139,274,627 REPS1
    nsv6817845copy number variation1nstd229human GRCh38 chr6: 138,948,301-138,950,400 , GRCh37.p13 chr6: 139,269,438-139,271,537 REPS1
    nsv6812631copy number variation1nstd229human GRCh38 chr6: 138,953,901-138,962,700 , GRCh37.p13 chr6: 139,275,038-139,283,837 REPS1
    nsv6811912copy number variation1nstd229human GRCh38 chr6: 137,801,388-140,356,633 , GRCh37.p13 chr6: 138,122,525-140,677,770 TXLNB, LOC100129844, 38 more genes
    nsv6810529copy number variation1nstd229human GRCh38 chr6: 138,913,545-138,927,432 , GRCh37.p13 chr6: 139,234,682-139,248,569 REPS1
    nsv6806179copy number variation1nstd229human GRCh38 chr6: 138,914,401-138,921,400 , GRCh37.p13 chr6: 139,235,538-139,242,537 REPS1
    nsv6805904copy number variation1nstd229human GRCh38 chr6: 138,967,308-138,975,717 , GRCh37.p13 chr6: 139,288,445-139,296,854 REPS1
    nsv6805031copy number variation1nstd229human GRCh38 chr6: 138,955,301-138,964,500 , GRCh37.p13 chr6: 139,276,438-139,285,637 REPS1
    nsv6802766copy number variation1nstd229human GRCh38 chr6: 138,941,201-138,953,500 , GRCh37.p13 chr6: 139,262,338-139,274,637 REPS1
    nsv6801360copy number variation1nstd229human GRCh38 chr6: 138,955,310-138,962,720 , GRCh37.p13 chr6: 139,276,447-139,283,857 REPS1
    nsv6799318copy number variation1nstd229human GRCh38 chr6: 138,966,224-138,967,280 , GRCh37.p13 chr6: 139,287,361-139,288,417 REPS1
    nsv6636436copy number variation1nstd102humanUncertain significance GRCh37 chr6: 139,063,032-139,273,184 , GRCh38.p12 chr6: 138,741,895-138,952,047 ECT2L, LOC107986650, 4 more genes
    nsv6615445copy number variation1nstd223human GRCh38 chr6: 138,883,585-138,902,621 , GRCh37.p13 chr6: 139,204,722-139,223,758 ECT2L, REPS1, 1 more genes
    nsv6614533copy number variation1nstd223human GRCh38 chr6: 138,985,301-138,991,700 , GRCh37.p13 chr6: 139,306,438-139,312,837 REPS1
    nsv6612094copy number variation1nstd223human GRCh38 chr6: 138,971,290-138,972,007 , GRCh37.p13 chr6: 139,292,427-139,293,144 REPS1
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