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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4945350copy number variation1nstd200human GRCh38 chr6: 81,691,926-82,286,650 , GRCh37.p13 chr6: 82,401,643-82,996,367 , LINC01526, 8 more genes
    nsv4566083mobile element insertion1nstd166human GRCh37.p13 chr6: 82,523,356-82,523,356 , GRCh38.p12 chr6: 81,813,639-81,813,639 LINC01526
    nsv4456122copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,216,253-82,753,743 , GRCh38.p12 chr6: 77,506,536-82,044,026 LOC105377869, AK4P5, 38 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 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
    nsv3911622copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 79,678,455-84,862,865 , GRCh37.p13 chr6: 79,621,736-84,806,146 , GRCh38.p12 chr6: 78,912,019-84,096,427 BCKDHB, DBIP1, 55 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 MRAP2, LCA5, 125 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
    nsv3872975copy number variation1nstd102humanPathogenic GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393 ME1, MTATP6P25, 178 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
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168753inversion1nstd158human GRCh37 chr6: 77,335,704-91,136,482 , GRCh38.p12 chr6: 76,625,987-90,426,763 , ACTBP8, 174 more genes
    nsv3168744inversion1nstd158human GRCh37 chr6: 81,126,432-158,470,478 , GRCh38.p12 chr6: 80,416,715-158,049,446 , ACTBP8, 985 more genes
    nsv3168209copy number variation1nstd158human GRCh38.p12 chr6: 56,099,235-128,190,528 , GRCh37 chr6: 55,964,033-128,511,673 , ACTBP8, 798 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
    nsv3168075inversion1nstd158human GRCh37 chr6: 10,515,049-82,678,331 , GRCh38.p12 chr6: 10,514,816-81,968,614 , ABCF1, 1617 more genes
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