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Items: 1 to 20 of 194

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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
    nsv7093981copy number variation2nstd102humanUncertain significance GRCh37 chr12: 8,800,687-8,814,700 , GRCh38.p12 chr12: 8,648,091-8,662,104 MFAP5
    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
    nsv6936633copy number variation1nstd229human GRCh38 chr12: 8,662,366-8,666,288 , GRCh37.p13 chr12: 8,814,962-8,818,884 MFAP5
    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
    nsv6923457copy number variation1nstd229human GRCh38 chr12: 8,656,521-8,661,896 , GRCh37.p13 chr12: 8,809,117-8,814,492 MFAP5
    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
    nsv6637627copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,781,515-9,605,163 , GRCh38.p12 chr12: 8,628,919-9,452,567 A2MP1, LOC101928030, 26 more genes
    nsv6463698copy number variation1nstd223human GRCh38 chr12: 8,651,209-8,655,026 , GRCh37.p13 chr12: 8,803,805-8,807,622 MFAP5
    nsv6460736copy number variation1nstd223human GRCh38 chr12: 8,656,793-8,659,364 , GRCh37.p13 chr12: 8,809,389-8,811,960 MFAP5
    nsv6309519copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,807,013-8,807,097 , GRCh38.p12 chr12: 8,654,417-8,654,501 MFAP5
    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
    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
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