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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705373mobile element insertion2nstd211human GRCh38 chr10: 56,361,746-56,361,746 , GRCh37.p13 chr10: 58,121,507-58,121,507 ZWINT
    nsv5635091insertion1nstd207human GRCh38 chr10: 56,361,732-56,361,732 , GRCh37.p13 chr10: 58,121,493-58,121,493 ZWINT
    nsv5490706copy number variation1nstd206human GRCh38 chr10: 56,275,910-56,400,064 , GRCh37.p13 chr10: 58,035,671-58,159,825 ZWINT
    nsv5402476mobile element insertion1nstd206human GRCh38 chr10: 56,361,746-56,361,797 , GRCh37.p13 chr10: 58,121,507-58,121,558 ZWINT
    nsv5347705translocation1nstd200human GRCh38 chr10: 56,361,323-56,361,323 , GRCh38 chr10: 56,361,250-56,361,250 , GRCh37.p13 chr10: 58,121,084-58,121,084 , GRCh37.p13 chr10: 58,121,011-58,121,011 ZWINT
    nsv5249195copy number variation1nstd204human GRCh38.p13 chr10: 56,352,601-56,357,300 , GRCh37.p13 chr10: 58,112,362-58,117,061 ZWINT
    nsv5138746mobile element insertion1nstd203human GRCh38 chr10: 56,361,732-56,361,746 , GRCh37.p13 chr10: 58,121,493-58,121,507 ZWINT
    nsv5126107mobile element insertion1nstd203human GRCh38 chr10: 56,361,737-56,361,746 , GRCh37.p13 chr10: 58,121,498-58,121,507 ZWINT
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973667copy number variation1nstd200human GRCh38 chr10: 56,361,649-56,411,241 , GRCh37.p13 chr10: 58,121,410-58,171,002 ZWINT
    nsv4970169copy number variation1nstd200human GRCh38 chr10: 56,205,064-56,671,862 , GRCh37.p13 chr10: 57,964,825-58,431,622 ZWINT
    nsv4970053copy number variation1nstd200human GRCh38 chr10: 53,834,085-56,369,996 , GRCh37.p13 chr10: 55,593,845-58,129,757 ZWINT, PCDH15, 7 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4846162copy number variation1nstd200human GRCh37 chr10: 57,964,825-58,431,622 , GRCh38.p12 chr10: 56,205,064-56,671,862 ZWINT
    nsv4835829copy number variation1nstd200human GRCh37 chr10: 58,121,410-58,171,002 , GRCh38.p12 chr10: 56,361,649-56,411,241 ZWINT
    nsv4728814copy number variation1nstd102humanLikely benign GRCh37 chr10: 57,590,896-58,861,610 , GRCh38.p12 chr10: 55,831,136-57,101,850 ZWINT
    nsv4675795copy number variation1nstd102humanPathogenic GRCh37 chr10: 55,589,950-63,990,649 , GRCh38.p12 chr10: 53,830,190-62,230,890 ARL4AP1, CABCOCO1, 52 more genes
    nsv4675630copy number variation1nstd102humanUncertain significance GRCh37 chr10: 57,969,989-59,123,710 , GRCh38.p12 chr10: 56,210,228-57,363,950 LOC105378313, ZWINT, 1 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4675436copy number variation1nstd102humanPathogenic GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638 MRPL35P2, MIR1296, 77 more genes
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