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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918284copy number variation1nstd209human GRCh38 chr10: 61,437,454-61,437,701 , GRCh37.p13 chr10: 63,197,212-63,197,459 TMEM26
    nsv5913413copy number variation1nstd209human GRCh38 chr10: 61,449,177-61,449,284 , GRCh37.p13 chr10: 63,208,935-63,209,042 TMEM26
    nsv5710603mobile element insertion2nstd211human GRCh38 chr10: 61,450,666-61,450,666 , GRCh37.p13 chr10: 63,210,424-63,210,424 TMEM26, TMEM26-AS1
    nsv5705567mobile element insertion1nstd211human GRCh38 chr10: 61,445,550-61,445,550 , GRCh37.p13 chr10: 63,205,308-63,205,308 TMEM26
    nsv5408285mobile element insertion1nstd206human GRCh38 chr10: 61,450,666-61,450,717 , GRCh37.p13 chr10: 63,210,424-63,210,475 TMEM26, TMEM26-AS1
    nsv5406466mobile element insertion1nstd206human GRCh38 chr10: 61,445,550-61,445,601 , GRCh37.p13 chr10: 63,205,308-63,205,359 TMEM26
    nsv5347755translocation1nstd200human GRCh38 chr10: 61,437,702-61,437,702 , GRCh38 chr10: 61,437,458-61,437,458 , GRCh37.p13 chr10: 63,197,216-63,197,216 , GRCh37.p13 chr10: 63,197,460-63,197,460 TMEM26
    nsv5242982copy number variation1nstd204human GRCh38.p13 chr10: 61,448,904-61,449,945 , GRCh37.p13 chr10: 63,208,662-63,209,703 TMEM26
    nsv5140024mobile element insertion1nstd203human GRCh38 chr10: 61,450,650-61,450,666 , GRCh37.p13 chr10: 63,210,408-63,210,424 TMEM26-AS1, TMEM26
    nsv5139969mobile element insertion1nstd203human GRCh38 chr10: 61,415,943-61,415,957 , GRCh37.p13 chr10: 63,175,701-63,175,715 TMEM26
    nsv5131503mobile element insertion1nstd203human GRCh38 chr10: 61,450,649-61,450,666 , GRCh37.p13 chr10: 63,210,407-63,210,424 TMEM26-AS1, TMEM26
    nsv5127389mobile element insertion1nstd203human GRCh38 chr10: 61,445,537-61,445,547 , GRCh37.p13 chr10: 63,205,295-63,205,305 TMEM26
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    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
    nsv4495007mobile element insertion1nstd166human GRCh37.p13 chr10: 63,205,295-63,205,295 , GRCh38.p12 chr10: 61,445,537-61,445,537 TMEM26
    nsv4482136mobile element insertion1nstd166human GRCh37.p13 chr10: 63,210,408-63,210,408 , GRCh38.p12 chr10: 61,450,650-61,450,650 TMEM26, TMEM26-AS1
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
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