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Items: 1 to 20 of 428

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114555mobile element insertion1nstd186human GRCh37 chr18: 9,401,421-9,401,472 , GRCh38.p12 chr18: 9,401,423-9,401,474 TWSG1
    nsv5977054insertion1nstd209human GRCh38 chr18: 9,401,405-9,401,405 , GRCh37.p13 chr18: 9,401,403-9,401,403 TWSG1
    nsv5968123insertion1nstd209human GRCh38 chr18: 9,344,530-9,344,530 , GRCh37.p13 chr18: 9,344,528-9,344,528 TWSG1
    nsv5938801copy number variation1nstd209human GRCh38 chr18: 9,368,540-9,372,202 , GRCh37.p13 chr18: 9,368,538-9,372,200 TWSG1
    nsv5938765copy number variation1nstd209human GRCh38 chr18: 9,385,393-9,385,716 , GRCh37.p13 chr18: 9,385,391-9,385,714 TWSG1
    nsv5870651copy number variation1nstd209human GRCh38 chr18: 9,368,521-9,371,655 , GRCh37.p13 chr18: 9,368,519-9,371,653 TWSG1
    nsv5709201mobile element insertion2nstd211human GRCh38 chr18: 9,401,423-9,401,423 , GRCh37.p13 chr18: 9,401,421-9,401,421 TWSG1
    nsv5697395mobile element insertion1nstd211human GRCh38 chr18: 9,355,384-9,355,384 , GRCh37.p13 chr18: 9,355,382-9,355,382 TWSG1
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5658294insertion1nstd207human GRCh38 chr18: 9,401,405-9,401,405 , GRCh37.p13 chr18: 9,401,403-9,401,403 TWSG1
    nsv5595123copy number variation1nstd207human GRCh38 chr18: 9,385,393-9,385,716 , GRCh37.p13 chr18: 9,385,391-9,385,714 TWSG1
    nsv5521875copy number variation1nstd206human GRCh38 chr18: 9,385,406-9,385,717 , GRCh37.p13 chr18: 9,385,404-9,385,715 TWSG1
    nsv5520806copy number variation1nstd206human GRCh38 chr18: 9,332,000-10,232,000 , GRCh37.p13 chr18: 9,331,998-10,231,997 RALBP1, RAB31, 21 more genes
    nsv5519567copy number variation1nstd206human GRCh38 chr18: 9,364,561-9,365,415 , GRCh37.p13 chr18: 9,364,559-9,365,413 TWSG1
    nsv5519131copy number variation1nstd206human GRCh38 chr18: 9,338,338-9,338,436 , GRCh37.p13 chr18: 9,338,336-9,338,434 TWSG1
    nsv5433333mobile element insertion1nstd206human GRCh38 chr18: 9,401,423-9,401,474 , GRCh37.p13 chr18: 9,401,421-9,401,472 TWSG1
    nsv5420787mobile element insertion1nstd206human GRCh38 chr18: 9,382,019-9,382,043 , GRCh37.p13 chr18: 9,382,017-9,382,041 TWSG1
    nsv5382853mobile element deletion2nstd186human GRCh37 chr18: 9,385,404-9,385,715 , GRCh38.p12 chr18: 9,385,406-9,385,717 TWSG1
    nsv5349857translocation1nstd200human GRCh38 chr18: 9,398,015-9,398,015 , GRCh38 chr18: 9,398,997-9,398,997 , GRCh37.p13 chr18: 9,398,995-9,398,995 , GRCh37.p13 chr18: 9,398,013-9,398,013 TWSG1
    nsv5349856translocation1nstd200human GRCh38 chr18: 9,396,546-9,396,546 , GRCh38 chr18: 9,399,343-9,399,343 , GRCh37.p13 chr18: 9,396,544-9,396,544 , GRCh37.p13 chr18: 9,399,341-9,399,341 TWSG1
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