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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv5037999inversion1nstd200human GRCh38 chr6: 85,122,647-85,919,417 , GRCh37.p13 chr6: 85,832,365-86,629,135 , LOC100127917, 19 more genes
    nsv4945377copy number variation1nstd200human GRCh38 chr6: 85,854,679-85,867,599 , GRCh37.p13 chr6: 86,564,397-86,577,317 LOC100133102
    nsv4945375copy number variation1nstd200human GRCh38 chr6: 85,831,954-86,431,566 , GRCh37.p13 chr6: 86,541,672-87,141,284 RPL7P27, LOC100652960, 5 more genes
    nsv4945373copy number variation1nstd200human GRCh38 chr6: 85,616,875-85,948,172 , GRCh37.p13 chr6: 86,326,593-86,657,890 , SYNCRIP, 9 more genes
    nsv4878533inversion1nstd200human GRCh37 chr6: 85,832,365-86,629,135 , GRCh38.p12 chr6: 85,122,647-85,919,417 , SNX14, 19 more genes
    nsv4824520copy number variation1nstd200human GRCh37 chr6: 86,541,672-87,141,284 , GRCh38.p12 chr6: 85,831,954-86,431,566 RPL7P27, RAB1AP2, 5 more genes
    nsv4685712copy number variation1nstd102humanUncertain significance GRCh37 chr6: 85,832,618-86,578,811 , GRCh38.p12 chr6: 85,122,900-85,869,093 PKMP3, LINC02535, 17 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv3960071copy number variation1nstd168human GRCh38 chr6: 85,833,863-85,873,906 , GRCh37.p13 chr6: 86,543,581-86,583,624 LOC100133102
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922883copy number variation1nstd102humanPathogenic NCBI36 chr6: 85,811,199-89,199,075 , GRCh37.p13 chr6: 85,754,480-89,142,356 , GRCh38.p12 chr6: 85,044,762-88,432,637 RN7SL643P, RPL7P27, 57 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
    nsv3918084copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697 LOC105377897, GABRR2, 91 more genes
    nsv3914763copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 85,693,301-88,131,878 , GRCh37 chr6: 85,636,582-88,075,159 , GRCh38 chr6: 84,926,864-87,365,441 CGA, HTR1E, 38 more genes
    nsv3914309copy number variation1nstd102humanPathogenic GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194 ME1, GJB7, 136 more genes
    nsv3912992copy number variation1nstd102humanPathogenic GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512 DNAJC19P6, RNU4-12P, 88 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
    nsv3889570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 85,770,403-87,222,520 , GRCh38.p12 chr6: 85,060,685-86,512,802 DUTP5, SNHG5, 24 more genes
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