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Items: 1 to 20 of 538

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    nsv6115422mobile element insertion1nstd186human GRCh37 chrY: 21,204,105-21,204,156 , GRCh38.p12 chrY: 19,042,219-19,042,270 TTTY14
    nsv5977488copy number variation1nstd209human GRCh38 chrY: 19,046,270-19,069,490 , GRCh37.p13 chrY: 21,208,156-21,231,376 TTTY14
    nsv5975856copy number variation1nstd209human GRCh38 chrY: 19,035,816-19,048,763 , GRCh37.p13 chrY: 21,197,702-21,210,649 TTTY14
    nsv5972539copy number variation2nstd209human GRCh38 chrY: 18,934,636-18,935,835 , GRCh37.p13 chrY: 21,096,522-21,097,721 TTTY14
    nsv5971240copy number variation1nstd209human GRCh38 chrY: 19,044,907-19,046,869 , GRCh37.p13 chrY: 21,206,793-21,208,755 TTTY14
    nsv5957039insertion1nstd209human GRCh38 chrY: 19,042,205-19,042,205 , GRCh37.p13 chrY: 21,204,091-21,204,091 TTTY14
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5562834sequence alteration1nstd206human GRCh38 chrY: 19,066,442-19,177,974 , GRCh37.p13 chrY: 21,228,328-21,339,860 TTTY14
    nsv5555198mobile element insertion1nstd206human GRCh38 chrY: 19,042,219-19,042,270 , GRCh37.p13 chrY: 21,204,105-21,204,156 TTTY14
    nsv5541060insertion1nstd206human GRCh38 chrY: 10,926,699-56,833,293 , GRCh37.p13 chrY: 13,193,955-58,979,440 , USP9YP18, 372 more genes
    nsv5432002copy number variation1nstd206human GRCh38 chrY: 17,451,387-18,881,388 , GRCh37.p13 chrY: 19,563,267-21,043,274 ACTG1P2, RNU1-95P, 75 more genes
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 more genes
    nsv5421022copy number variation1nstd206human GRCh38 chrY: 18,869,638-18,878,788 , GRCh37.p13 chrY: 21,031,524-21,040,674 MTCYBP2, TTTY14
    nsv5419558copy number variation1nstd206human GRCh38 chrY: 18,452,123-19,040,123 , GRCh37.p13 chrY: 20,614,009-21,202,009 HSFY2, ELOCP14, 28 more genes
    nsv5355484translocation1nstd200human GRCh38 chrY: 18,953,409-18,953,409 , GRCh38 chr11: 116,528,409-116,528,409 , GRCh37.p13 chr11: 116,399,126-116,399,126 , GRCh37.p13 chrY: 21,115,295-21,115,295 TTTY14
    nsv5355483translocation1nstd200human GRCh38 chr11: 116,528,406-116,528,406 , GRCh38 chrY: 18,953,266-18,953,266 , GRCh37.p13 chr11: 116,399,123-116,399,123 , GRCh37.p13 chrY: 21,115,152-21,115,152 TTTY14
    nsv5336188translocation1nstd200human GRCh37 chr14: 45,935,188-45,935,188 , GRCh37 chrY: 21,154,679-21,154,679 , GRCh38.p12 chr14: 45,465,985-45,465,985 , GRCh38.p12 chrY: 18,992,793-18,992,793 CD24P4, TTTY14, 1 more genes
    nsv5200089mobile element insertion1nstd203human GRCh38 chrY: 19,042,210-19,042,218 , GRCh37.p13 chrY: 21,204,096-21,204,104 TTTY14
    nsv5200088mobile element insertion1nstd203human GRCh38 chrY: 19,042,209-19,042,219 , GRCh37.p13 chrY: 21,204,095-21,204,105 TTTY14
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