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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5683620mobile element insertion1nstd211human GRCh38 chr6: 19,143,133-19,143,133 , GRCh37.p13 chr6: 19,143,364-19,143,364 LOC101928519, RPL21P61
    nsv5412721mobile element insertion1nstd206human GRCh38 chr6: 19,143,133-19,143,184 , GRCh37.p13 chr6: 19,143,364-19,143,415 LOC101928519, RPL21P61
    nsv4933001copy number variation1nstd200human GRCh38 chr6: 19,139,349-19,148,283 , GRCh37.p13 chr6: 19,139,580-19,148,514 RPL21P61, LOC101928519
    nsv4809929copy number variation1nstd200human GRCh37 chr6: 19,139,580-19,148,514 , GRCh38.p12 chr6: 19,139,349-19,148,283 RPL21P61, LOC101928519
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456299copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,910,125-22,000,204 , GRCh38.p12 chr6: 13,909,894-21,999,975 LOC101928354, MBOAT1, 101 more genes
    nsv4115110copy number variation1nstd166human GRCh37.p13 chr6: 19,139,580-19,148,514 , GRCh38.p12 chr6: 19,139,349-19,148,283 LOC101928519, RPL21P61
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3888615copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006 LOC107986557, PXDC1, 349 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3886069copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-21,955,964 , GRCh38.p12 chr6: 156,974-21,955,733 FOXCUT, ACCSLP1, 331 more genes
    nsv3882845copy number variation1nstd102humanUncertain significance GRCh37 chr6: 18,576,869-19,218,841 , GRCh38.p12 chr6: 18,576,638-19,218,610 LOC101928519, MIR548A1HG, 4 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3875604copy number variation1nstd102humanPathogenic GRCh37 chr6: 13,693,852-24,225,515 , GRCh38.p12 chr6: 13,693,620-24,225,287 KIF13A, PRL, 124 more genes
    nsv3872568copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,775-24,023,234 , GRCh38.p12 chr6: 168,775-24,023,006 TXNDC5, JARID2, 349 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
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