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Items: 1 to 20 of 173

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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
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 more genes
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6933060copy number variation1nstd229human GRCh38 chr12: 8,609,439-8,621,956 , GRCh37.p13 chr12: 8,762,035-8,774,552 AICDA
    nsv6931924copy number variation1nstd229human GRCh38 chr12: 8,588,747-8,885,593 , GRCh37.p13 chr12: 8,741,343-9,038,189 RPSAP51, RIMKLB, 5 more genes
    nsv6930590copy number variation1nstd229human GRCh38 chr12: 8,482,988-8,890,232 , GRCh37.p13 chr12: 8,635,584-9,042,828 A2ML1, LOC105369645, 10 more genes
    nsv6922975copy number variation1nstd229human GRCh38 chr12: 8,496,095-8,678,952 , GRCh37.p13 chr12: 8,648,691-8,831,548 CLEC4D, LOC105369645, 6 more genes
    nsv6580726inversion1nstd223human GRCh38 chr12: 8,607,902-8,608,407 , GRCh37.p13 chr12: 8,760,498-8,761,003 AICDA
    nsv6460948copy number variation1nstd223human GRCh38 chr12: 8,311,354-8,628,664 , GRCh37.p13 chr12: 8,463,950-8,781,260 AICDA, OR7E140P, 14 more genes
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309328copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,978,008-9,010,204 , GRCh38.p12 chr12: 6,868,844-8,857,608 LOC101927966, SNRPCP7, 87 more genes
    nsv6285327insertion2nstd214human GRCh38 chr12: 8,608,228-8,608,228 , GRCh37.p13 chr12: 8,760,824-8,760,824 AICDA
    nsv6132718copy number variation1nstd213human GRCh37 chr12: 8,640,000-9,100,001 , GRCh38.p12 chr12: 8,487,404-8,947,405 A2ML1, RPSAP51, 11 more genes
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6100169insertion1nstd212human GRCh38 chr12: 8,608,257-8,608,257 , GRCh37.p13 chr12: 8,760,853-8,760,853 AICDA
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