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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977899inversion1nstd209human GRCh38 chr2: 227,539,323-230,369,909 , GRCh37.p13 chr2: 228,404,039-231,234,624 , AGFG1, 40 more genes
    nsv5902172copy number variation1nstd209human GRCh38 chr2: 230,310,337-230,400,551 , GRCh37.p13 chr2: 231,175,052-231,265,266 SP140, SP140L, 1 more genes
    nsv5682758mobile element insertion2nstd211human GRCh38 chr2: 230,308,399-230,308,399 , GRCh37.p13 chr2: 231,173,114-231,173,114 SP140
    nsv5675070mobile element insertion2nstd211human GRCh38 chr2: 230,252,768-230,252,768 , GRCh37.p13 chr2: 231,117,483-231,117,483 SP140
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5548988insertion1nstd206human GRCh38 chr2: 230,252,768-230,252,819 , GRCh37.p13 chr2: 231,117,483-231,117,534 SP140
    nsv5449024copy number variation1nstd206human GRCh38 chr2: 228,447,618-230,410,000 , GRCh37.p13 chr2: 229,312,334-231,274,715 , RPL7L1P10, 25 more genes
    nsv5394052mobile element insertion1nstd206human GRCh38 chr2: 230,308,399-230,308,450 , GRCh37.p13 chr2: 231,173,114-231,173,165 SP140
    nsv5351183translocation1nstd200human GRCh38 chr2: 230,206,567-230,206,567 , GRCh38 chr2: 230,206,634-230,206,634 , GRCh37.p13 chr2: 231,071,282-231,071,282 , GRCh37.p13 chr2: 231,071,349-231,071,349 SP110, SP140
    nsv5314204copy number variation1nstd204human GRCh37.p13 chr2: 231,071,250-231,075,896 , GRCh38.p13 chr2: 230,206,535-230,211,181 SP110, SP140
    nsv5309322copy number variation1nstd204human GRCh37.p13 chr2: 231,068,226-231,070,733 , GRCh38.p13 chr2: 230,203,510-230,206,018 SP110, SP140
    nsv5200403copy number variation1nstd204human GRCh38.p13 chr2: 230,203,476-230,210,754 , GRCh37.p13 chr2: 231,068,192-231,075,469 SP140, SP110
    nsv5077026mobile element insertion1nstd203human GRCh38 chr2: 230,308,382-230,308,399 , GRCh37.p13 chr2: 231,173,097-231,173,114 SP140
    nsv5074303mobile element insertion1nstd203human GRCh38 chr2: 230,252,756-230,252,768 , GRCh37.p13 chr2: 231,117,471-231,117,483 SP140
    nsv5071112mobile element insertion1nstd203human GRCh38 chr2: 230,276,989-230,277,004 , GRCh37.p13 chr2: 231,141,704-231,141,719 SP140
    nsv5067436mobile element insertion1nstd203human GRCh38 chr2: 230,252,751-230,252,768 , GRCh37.p13 chr2: 231,117,466-231,117,483 SP140
    nsv5066935mobile element insertion1nstd203human GRCh38 chr2: 230,252,752-230,252,768 , GRCh37.p13 chr2: 231,117,467-231,117,483 SP140
    nsv5061532mobile element insertion1nstd203human GRCh38 chr2: 230,252,753-230,252,768 , GRCh37.p13 chr2: 231,117,468-231,117,483 SP140
    nsv5039254inversion1nstd200human GRCh38 chr2: 227,539,122-230,370,113 , GRCh37.p13 chr2: 228,403,838-231,234,828 , LOC105373921, 40 more genes
    nsv4914028copy number variation1nstd200human GRCh38 chr2: 230,180,467-230,272,344 , GRCh37.p13 chr2: 231,045,183-231,137,059 SP110, SP140
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