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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961744insertion1nstd209human GRCh38 chr6: 22,141,994-22,141,994 , GRCh37.p13 chr6: 22,142,223-22,142,223 NBAT1, CASC15
    nsv5714595mobile element insertion1nstd211human GRCh38 chr6: 22,132,632-22,132,632 , GRCh37.p13 chr6: 22,132,861-22,132,861 CASC15, NBAT1
    nsv5090059mobile element insertion1nstd203human GRCh38 chr6: 22,145,866-22,145,882 , GRCh37.p13 chr6: 22,146,095-22,146,111 CASC15, NBAT1
    nsv5030523inversion1nstd200human GRCh38 chr6: 21,391,567-22,908,554 , GRCh37.p13 chr6: 21,391,798-22,908,783 LINC00581, HDGFL1, 12 more genes
    nsv4934508copy number variation1nstd200human GRCh38 chr6: 22,144,342-22,151,878 , GRCh37.p13 chr6: 22,144,571-22,152,107 CASC15, NBAT1
    nsv4933135copy number variation1nstd200human GRCh38 chr6: 22,135,608-22,138,377 , GRCh37.p13 chr6: 22,135,837-22,138,606 NBAT1, CASC15
    nsv4828543copy number variation1nstd200human GRCh37 chr6: 22,144,571-22,152,107 , GRCh38.p12 chr6: 22,144,342-22,151,878 CASC15, NBAT1
    nsv4815574copy number variation1nstd200human GRCh37 chr6: 22,135,837-22,138,606 , GRCh38.p12 chr6: 22,135,608-22,138,377 NBAT1, CASC15
    nsv4482881mobile element insertion1nstd166human GRCh37.p13 chr6: 22,141,727-22,141,727 , GRCh38.p12 chr6: 22,141,498-22,141,498 CASC15, NBAT1
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv3961142copy number variation1nstd168human GRCh38 chr6: 22,134,464-22,207,098 , GRCh37.p13 chr6: 22,134,693-22,207,327 NBAT1, CASC15
    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
    nsv3885889copy number variation1nstd102humanBenign GRCh37 chr6: 21,972,800-22,161,904 , GRCh38.p12 chr6: 21,972,569-22,161,675 RN7SKP240, NBAT1, 1 more genes
    nsv3883900copy number variation1nstd102humanUncertain significance GRCh37 chr6: 21,288,478-22,264,251 , GRCh38.p12 chr6: 21,288,247-22,264,022 SOX4, CASC15, 6 more genes
    nsv3881737copy number variation1nstd102humanBenign GRCh37 chr6: 22,122,568-22,133,359 , GRCh38.p12 chr6: 22,122,339-22,133,130 NBAT1, CASC15
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
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