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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917513copy number variation1nstd209human GRCh38 chr10: 61,458,185-61,458,257 , GRCh37.p13 chr10: 63,217,943-63,218,015 TMEM26-AS1
    nsv5710603mobile element insertion2nstd211human GRCh38 chr10: 61,450,666-61,450,666 , GRCh37.p13 chr10: 63,210,424-63,210,424 TMEM26, TMEM26-AS1
    nsv5627459insertion1nstd207human GRCh38 chr10: 61,458,185-61,458,185 , GRCh37.p13 chr10: 63,217,943-63,217,943 TMEM26-AS1
    nsv5596005copy number variation1nstd207human GRCh38 chr10: 61,491,261-61,491,431 , GRCh37.p13 chr10: 63,251,019-63,251,189 TMEM26-AS1
    nsv5479991copy number variation1nstd206human GRCh38 chr10: 61,466,750-61,466,813 , GRCh37.p13 chr10: 63,226,508-63,226,571 TMEM26-AS1
    nsv5408285mobile element insertion1nstd206human GRCh38 chr10: 61,450,666-61,450,717 , GRCh37.p13 chr10: 63,210,424-63,210,475 TMEM26, TMEM26-AS1
    nsv5140024mobile element insertion1nstd203human GRCh38 chr10: 61,450,650-61,450,666 , GRCh37.p13 chr10: 63,210,408-63,210,424 TMEM26-AS1, TMEM26
    nsv5131503mobile element insertion1nstd203human GRCh38 chr10: 61,450,649-61,450,666 , GRCh37.p13 chr10: 63,210,407-63,210,424 TMEM26-AS1, TMEM26
    nsv5126954mobile element insertion1nstd203human GRCh38 chr10: 61,458,646-61,458,660 , GRCh37.p13 chr10: 63,218,404-63,218,418 TMEM26-AS1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4975982copy number variation1nstd200human GRCh38 chr10: 61,462,950-61,465,329 , GRCh37.p13 chr10: 63,222,708-63,225,087 TMEM26-AS1
    nsv4751076insertion1nstd199human GRCh37 chr10: 63,217,982-63,217,982 , GRCh38.p12 chr10: 61,458,224-61,458,224 TMEM26-AS1
    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
    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
    nsv4674969copy number variation1nstd102humanUncertain significance GRCh37 chr10: 62,191,184-65,348,431 , GRCh38.p12 chr10: 60,431,426-63,588,671 RNU6-543P, ARID5B, 33 more genes
    nsv4636331copy number variation1nstd186human GRCh37 chr10: 63,217,943-63,218,017 , GRCh38.p12 chr10: 61,458,185-61,458,259 TMEM26-AS1
    nsv4612610copy number variation1nstd183human GRCh37 chr10: 63,236,587-63,247,795 , GRCh38.p12 chr10: 61,476,829-61,488,037 TMEM26-AS1
    nsv4605701copy number variation1nstd183human GRCh37 chr10: 63,216,707-63,242,227 , GRCh38.p12 chr10: 61,456,949-61,482,469 TMEM26-AS1
    nsv4576765mobile element insertion1nstd166human GRCh37.p13 chr10: 63,218,303-63,218,303 , GRCh38.p12 chr10: 61,458,545-61,458,545 TMEM26-AS1
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