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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5460471copy number variation1nstd206human GRCh38 chr6: 31,119,831-31,186,318 , GRCh37.p13 chr6: 31,087,608-31,154,095 CDSN, POU5F1, 6 more genes
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5183368mobile element insertion1nstd203human GRCh38 chr6: 31,168,500-31,168,516 , GRCh37.p13 chr6: 31,136,277-31,136,293 POU5F1
    nsv4828596copy number variation1nstd200human GRCh37 chr6: 31,087,555-31,154,139 , GRCh38.p12 chr6: 31,119,778-31,186,362 PSORS1C3, POU5F1, 6 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4728012copy number variation4nstd197human GRCh37 chr6: 31,083,803-31,133,824 , GRCh38.p12 chr6: 31,116,026-31,166,047 CDSN, POU5F1, 5 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4646502copy number variation1nstd186human GRCh37 chr6: 31,131,451-31,272,307 , GRCh38.p12 chr6: 31,163,674-31,304,530 POU5F1, PSORS1C3, 8 more genes
    nsv4436473complex substitution1nstd102humanUncertain significance GRCh38.p12 chr6: 31,117,423-31,356,870 , GRCh37 chr6: 31,085,200-31,324,647 CDSN, HLA-B, 15 more genes
    nsv4403147copy number variation1nstd174human GRCh37 chr6: 30,372,579-31,314,243 , GRCh38.p12 chr6: 30,404,802-31,346,466 MIR4640, NAPGP2, 58 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 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
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 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
    nsv3870570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590 LOC105375002, SKIC2, 345 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
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