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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055605inversion1nstd229human GRCh38 chr6: 149,922,042-149,952,296 , GRCh37.p13 chr6: 150,243,178-150,273,432 ULBP2, RAET1G, 1 more genes
    nsv7052718inversion1nstd229human GRCh38 chr6: 149,810,140-150,026,610 , GRCh37.p13 chr6: 150,131,276-150,347,746 RAET1E, RAET1G, 12 more genes
    nsv7050118inversion1nstd229human GRCh38 chr6: 149,858,013-149,990,866 , GRCh37.p13 chr6: 150,179,149-150,312,002 ULBP2, RAET1E, 9 more genes
    nsv7046609inversion1nstd229human GRCh38 chr6: 149,890,209-149,943,198 , GRCh37.p13 chr6: 150,211,345-150,264,334 RAET1E, RAET1F, 5 more genes
    nsv7044040inversion1nstd229human GRCh38 chr6: 149,831,135-150,057,336 , GRCh37.p13 chr6: 150,152,271-150,378,472 RAET1M, RAET1E, 13 more genes
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv6817117copy number variation1nstd229human GRCh38 chr6: 149,880,977-150,003,393 , GRCh37.p13 chr6: 150,202,113-150,324,529 RAET1E, LOC100240714, 9 more genes
    nsv6815049copy number variation1nstd229human GRCh38 chr6: 149,923,484-149,941,214 , GRCh37.p13 chr6: 150,244,620-150,262,350 ULBP2, RAET1G, 1 more genes
    nsv6802206copy number variation1nstd229human GRCh38 chr6: 149,934,307-149,934,517 , GRCh37.p13 chr6: 150,255,443-150,255,653 LOC105378052
    nsv6603600copy number variation1nstd223human GRCh38 chr6: 149,930,549-149,949,635 , GRCh37.p13 chr6: 150,251,685-150,270,771 LOC105378052, ULBP2
    nsv6600797copy number variation1nstd223human GRCh38 chr6: 149,921,947-150,024,548 , GRCh37.p13 chr6: 150,243,083-150,345,684 ULBP1, RAET1L, 5 more genes
    nsv6600468copy number variation1nstd223human GRCh38 chr6: 149,933,145-149,982,614 , GRCh37.p13 chr6: 150,254,281-150,303,750 LOC105378052, ULBP1, 2 more genes
    nsv6571422inversion1nstd223human GRCh38 chr6: 146,996,555-151,115,323 , GRCh37.p13 chr6: 147,317,691-151,436,459 RPSAP40, STXBP5, 62 more genes
    nsv6136476copy number variation1nstd213human GRCh37 chr6: 150,140,000-151,440,001 , GRCh38.p12 chr6: 149,818,864-151,118,865 PHB1P1, LRP11, 27 more genes
    nsv5461928copy number variation1nstd206human GRCh38 chr6: 149,930,470-149,949,732 , GRCh37.p13 chr6: 150,251,606-150,270,868 LOC105378052, ULBP2
    nsv4943350copy number variation1nstd200human GRCh38 chr6: 149,930,538-149,949,647 , GRCh37.p13 chr6: 150,251,674-150,270,783 LOC105378052, ULBP2
    nsv4810872copy number variation1nstd200human GRCh37 chr6: 150,251,652-150,270,802 , GRCh38.p12 chr6: 149,930,516-149,949,666 ULBP2, LOC105378052
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4436722copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,690,764-150,494,873 , GRCh38.p12 chr6: 148,369,628-150,173,737 PCMT1, ULBP3, 42 more genes
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