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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7076787inversion1nstd229human GRCh38 chr12: 31,508,119-31,914,238 , GRCh37.p13 chr12: 31,661,053-32,067,172 RNU6-1069P, RPL31P50, 14 more genes
    nsv7068504inversion1nstd229human GRCh38 chr12: 31,640,473-31,676,490 , GRCh37.p13 chr12: 31,793,407-31,829,424 AMN1, ETFBKMT
    nsv6937987copy number variation1nstd229human GRCh38 chr12: 31,645,141-31,645,202 , GRCh37.p13 chr12: 31,798,075-31,798,136 ETFBKMT
    nsv6920449copy number variation1nstd229human GRCh38 chr12: 31,645,849-31,646,247 , GRCh37.p13 chr12: 31,798,783-31,799,181 ETFBKMT
    nsv6621604copy number variation1nstd224human GRCh37 chr12: 31,819,105-31,945,000 , GRCh38.p12 chr12: 31,666,171-31,792,066 IFITM3P2, AMN1, 6 more genes
    nsv6589904inversion1nstd223human GRCh38 chr12: 31,653,730-31,654,275 , GRCh37.p13 chr12: 31,806,664-31,807,209 ETFBKMT
    nsv6580523inversion1nstd223human GRCh38 chr12: 31,653,825-31,654,220 , GRCh37.p13 chr12: 31,806,759-31,807,154 ETFBKMT
    nsv6468398copy number variation1nstd223human GRCh38 chr12: 31,646,599-31,648,930 , GRCh37.p13 chr12: 31,799,533-31,801,864 ETFBKMT
    nsv6467967copy number variation1nstd223human GRCh38 chr12: 31,648,825-31,650,016 , GRCh37.p13 chr12: 31,801,759-31,802,950 ETFBKMT
    nsv6461547copy number variation1nstd223human GRCh38 chr12: 31,648,916-31,651,515 , GRCh37.p13 chr12: 31,801,850-31,804,449 ETFBKMT
    nsv6458516copy number variation1nstd223human GRCh38 chr12: 31,671,567-31,671,968 , GRCh37.p13 chr12: 31,824,501-31,824,902 AMN1, ETFBKMT
    nsv6240880mobile element insertion1nstd215human GRCh38 chr12: 31,650,642-31,650,642 , GRCh37.p13 chr12: 31,803,576-31,803,576 ETFBKMT
    nsv6132241copy number variation1nstd213human GRCh37 chr12: 31,410,000-34,000,001 , GRCh38.p12 chr12: 31,257,066-33,847,066 ASS1P14, BICD1, 39 more genes
    nsv6097913insertion1nstd212human GRCh38 chr12: 31,650,025-31,650,025 , GRCh37.p13 chr12: 31,802,959-31,802,959 ETFBKMT
    nsv6093820insertion1nstd212human GRCh38 chr12: 31,666,084-31,666,084 , GRCh37.p13 chr12: 31,819,018-31,819,018 ETFBKMT
    nsv6038011copy number variation1nstd212human GRCh38 chr12: 31,639,019-31,646,171 , GRCh37.p13 chr12: 31,791,953-31,799,105 ETFBKMT
    nsv6029747copy number variation1nstd212human GRCh38 chr12: 31,640,701-31,647,573 , GRCh37.p13 chr12: 31,793,635-31,800,507 ETFBKMT
    nsv5978493insertion1nstd209human GRCh38 chr12: 31,650,025-31,650,025 , GRCh37.p13 chr12: 31,802,959-31,802,959 ETFBKMT
    nsv5909629copy number variation1nstd209human GRCh38 chr12: 31,646,564-31,648,929 , GRCh37.p13 chr12: 31,799,498-31,801,863 ETFBKMT
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