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Items: 1 to 20 of 79

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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
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4934164copy number variation1nstd200human GRCh38 chr6: 132,553,488-132,570,833 , GRCh37.p13 chr6: 132,874,627-132,891,972 TAAR7P, TAAR8, 1 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
    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
    nsv3914780copy number variation1nstd102humanUncertain significance NCBI36 chr6: 132,860,706-132,969,136 , GRCh37.p13 chr6: 132,819,013-132,927,443 , GRCh38.p12 chr6: 132,497,874-132,606,304 TAAR8, TAAR6, 7 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
    nsv3906356copy number variation1nstd102humanUncertain significance GRCh37 chr6: 132,859,724-132,910,636 , GRCh38.p12 chr6: 132,538,585-132,589,497 TAAR5, TAAR9, 3 more genes
    nsv3904160copy number variation1nstd102humanBenign GRCh37 chr6: 132,794,904-132,879,258 , GRCh38.p12 chr6: 132,473,765-132,558,119 TAAR9, STX7, 3 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
    esv4011098complex chromosomal rearrangement4estd236human GRCh37 chr6: 48,385,249-154,434,404 , GRCh38.p12 chr6: 48,417,513-154,113,269 , ACTBP8, 1274 more genes
    nsv3168744inversion1nstd158human GRCh37 chr6: 81,126,432-158,470,478 , GRCh38.p12 chr6: 80,416,715-158,049,446 , ACTBP8, 985 more genes
    nsv3168167copy number variation1nstd158human GRCh37 chr6: 12,299,904-158,472,787 , GRCh38.p12 chr6: 12,299,671-158,051,755 , ABCF1, 2551 more genes
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