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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
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5891523copy number variation1nstd209human GRCh38 chr6: 132,618,937-132,629,308 , GRCh37.p13 chr6: 132,940,076-132,950,447 TAAR2
    nsv5843757copy number variation1nstd209human GRCh38 chr6: 132,618,823-132,629,232 , GRCh37.p13 chr6: 132,939,962-132,950,371 TAAR2
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4934167copy number variation1nstd200human GRCh38 chr6: 132,618,939-132,629,309 , GRCh37.p13 chr6: 132,940,078-132,950,448 TAAR2
    nsv4826503copy number variation1nstd200human GRCh37 chr6: 132,940,078-132,950,448 , GRCh38.p12 chr6: 132,618,939-132,629,309 TAAR2
    nsv4495428mobile element insertion1nstd166human GRCh37.p13 chr6: 132,945,740-132,945,740 , GRCh38.p12 chr6: 132,624,601-132,624,601 TAAR2
    nsv4456756copy number variation1nstd102humanUncertain significance GRCh37 chr6: 132,926,920-133,314,722 , GRCh38.p12 chr6: 132,605,781-132,993,583 HMGB1P13, SLC18B1, 15 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4146523copy number variation1nstd166human GRCh37.p13 chr6: 132,940,078-132,950,448 , GRCh38.p12 chr6: 132,618,939-132,629,309 TAAR2
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 more genes
    nsv3913212copy number variation1nstd102humanUncertain significance GRCh37 chr6: 132,776,411-133,462,292 , GRCh38 chr6: 132,455,272-133,141,153 , NCBI36 chr6: 132,818,104-133,503,985 TAAR5, TAAR9, 25 more genes
    nsv3893875copy number variation1nstd102humanPathogenic GRCh37 chr6: 132,002,460-137,160,850 , GRCh38.p12 chr6: 131,681,320-136,839,712 TAAR9, EEF1A1P36, 93 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
    nsv3871408copy number variation1nstd102humanPathogenic GRCh37 chr6: 131,388,023-137,469,640 , GRCh38.p12 chr6: 131,066,883-137,148,503 LOC105378012, MIR3662, 108 more genes
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