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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
    nsv6125371insertion1nstd186human GRCh37 chrX: 138,744,466-138,744,466 , GRCh38.p12 chrX: 139,662,307-139,662,307 MCF2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5874005copy number variation1nstd209human GRCh38 chrX: 139,616,751-139,616,827 , GRCh37.p13 chrX: 138,698,910-138,698,986 MCF2
    nsv5728852mobile element insertion2nstd211human GRCh38 chrX: 139,596,904-139,596,904 , GRCh37.p13 chrX: 138,679,063-138,679,063 MCF2
    nsv5727772mobile element insertion1nstd211human GRCh38 chrX: 139,599,652-139,599,652 , GRCh37.p13 chrX: 138,681,811-138,681,811 MCF2
    nsv5724968mobile element insertion2nstd211human GRCh38 chrX: 139,689,654-139,689,654 , GRCh37.p13 chrX: 138,771,813-138,771,813 MCF2
    nsv5715800mobile element insertion1nstd211human GRCh38 chrX: 139,595,858-139,595,858 , GRCh37.p13 chrX: 138,678,017-138,678,017 MCF2
    nsv5715390mobile element insertion2nstd211human GRCh38 chrX: 139,662,323-139,662,323 , GRCh37.p13 chrX: 138,744,482-138,744,482 MCF2
    nsv5612055insertion1nstd207human GRCh38 chrX: 139,662,307-139,662,307 , GRCh37.p13 chrX: 138,744,466-138,744,466 MCF2
    nsv5561843mobile element insertion1nstd206human GRCh38 chrX: 139,599,652-139,599,703 , GRCh37.p13 chrX: 138,681,811-138,681,862 MCF2
    nsv5556438mobile element insertion1nstd206human GRCh38 chrX: 139,689,654-139,689,699 , GRCh37.p13 chrX: 138,771,813-138,771,858 MCF2
    nsv5545230insertion1nstd206human GRCh38 chrX: 139,581,189-139,581,192 , GRCh37.p13 chrX: 138,663,348-138,663,351 MCF2
    nsv5540820insertion1nstd206human GRCh38 chrX: 139,662,307-139,662,307 , GRCh37.p13 chrX: 138,744,466-138,744,466 MCF2
    nsv5377157translocation1nstd200human GRCh38 chrX: 139,943,986-139,943,986 , GRCh38 chrX: 139,646,026-139,646,026 , GRCh37.p13 chrX: 139,026,145-139,026,145 , GRCh37.p13 chrX: 138,728,185-138,728,185 MCF2
    nsv5377156translocation1nstd200human GRCh38 chrX: 139,591,723-139,591,723 , GRCh38 chrX: 139,557,770-139,557,770 , GRCh37.p13 chrX: 138,639,929-138,639,929 , GRCh37.p13 chrX: 138,673,882-138,673,882 F9, MCF2
    nsv5341444translocation1nstd200human GRCh37 chrX: 139,026,145-139,026,145 , GRCh37 chrX: 138,728,185-138,728,185 , GRCh38.p12 chrX: 139,646,026-139,646,026 , GRCh38.p12 chrX: 139,943,986-139,943,986 MCF2
    nsv5195369mobile element insertion1nstd203human GRCh38 chrX: 139,659,471-139,659,486 , GRCh37.p13 chrX: 138,741,630-138,741,645 MCF2
    nsv5192234mobile element insertion1nstd203human GRCh38 chrX: 139,695,902-139,695,913 , GRCh37.p13 chrX: 138,778,061-138,778,072 MCF2
    nsv5190914mobile element insertion1nstd203human GRCh38 chrX: 139,662,307-139,662,323 , GRCh37.p13 chrX: 138,744,466-138,744,482 MCF2
    nsv5186265mobile element insertion1nstd203human GRCh38 chrX: 139,689,643-139,689,654 , GRCh37.p13 chrX: 138,771,802-138,771,813 MCF2
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