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Items: 1 to 20 of 557

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7097050copy number variation2nstd102humanPathogenic GRCh37 chr6: 158,532,398-162,868,359 , GRCh38.p12 chr6: 158,111,366-162,447,327 LOC107986665, HNRNPH1P1, 64 more genes
    nsv7049245inversion1nstd229human GRCh38 chr6: 161,099,889-161,129,329 , GRCh37.p13 chr6: 161,520,921-161,550,361 MAP3K4, AGPAT4
    nsv7045323inversion1nstd229human GRCh38 chr6: 161,129,850-161,138,723 , GRCh37.p13 chr6: 161,550,882-161,559,755 AGPAT4
    nsv6817994copy number variation1nstd229human GRCh38 chr6: 161,256,801-161,265,800 , GRCh37.p13 chr6: 161,677,833-161,686,832 AGPAT4
    nsv6816370copy number variation1nstd229human GRCh38 chr6: 161,145,226-161,145,831 , GRCh37.p13 chr6: 161,566,258-161,566,863 AGPAT4
    nsv6815479copy number variation1nstd229human GRCh38 chr6: 161,265,629-161,265,770 , GRCh37.p13 chr6: 161,686,661-161,686,802 AGPAT4
    nsv6815051copy number variation1nstd229human GRCh38 chr6: 161,263,105-161,263,206 , GRCh37.p13 chr6: 161,684,137-161,684,238 AGPAT4
    nsv6814676copy number variation1nstd229human GRCh38 chr6: 161,254,767-161,258,464 , GRCh37.p13 chr6: 161,675,799-161,679,496 AGPAT4
    nsv6814605copy number variation1nstd229human GRCh38 chr6: 161,130,068-161,132,677 , GRCh37.p13 chr6: 161,551,100-161,553,709 AGPAT4
    nsv6813721copy number variation1nstd229human GRCh38 chr6: 161,191,334-161,195,565 , GRCh37.p13 chr6: 161,612,366-161,616,597 AGPAT4
    nsv6813167copy number variation1nstd229human GRCh38 chr6: 161,195,783-161,198,901 , GRCh37.p13 chr6: 161,616,815-161,619,933 AGPAT4
    nsv6813078copy number variation1nstd229human GRCh38 chr6: 161,237,676-161,238,028 , GRCh37.p13 chr6: 161,658,708-161,659,060 AGPAT4
    nsv6812472copy number variation1nstd229human GRCh38 chr6: 161,245,675-161,251,101 , GRCh37.p13 chr6: 161,666,707-161,672,133 AGPAT4
    nsv6811930copy number variation1nstd229human GRCh38 chr6: 161,256,822-161,265,853 , GRCh37.p13 chr6: 161,677,854-161,686,885 AGPAT4
    nsv6811334copy number variation1nstd229human GRCh38 chr6: 161,121,705-161,128,409 , GRCh37.p13 chr6: 161,542,737-161,549,441 AGPAT4
    nsv6810427copy number variation1nstd229human GRCh38 chr6: 161,054,835-161,169,282 , GRCh37.p13 chr6: 161,475,867-161,590,314 MAP3K4, AGPAT4, 1 more genes
    nsv6809369copy number variation1nstd229human GRCh38 chr6: 161,196,490-161,203,954 , GRCh37.p13 chr6: 161,617,522-161,624,986 AGPAT4
    nsv6807968copy number variation1nstd229human GRCh38 chr6: 161,208,292-161,223,485 , GRCh37.p13 chr6: 161,629,324-161,644,517 AGPAT4
    nsv6807439copy number variation1nstd229human GRCh38 chr6: 161,193,585-161,193,955 , GRCh37.p13 chr6: 161,614,617-161,614,987 AGPAT4
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