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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv7064051inversion1nstd229human GRCh38 chr8: 53,370,406-56,357,942 , GRCh37.p13 chr8: 54,282,966-57,270,501 CHCHD2P10, RN7SL798P, 51 more genes
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6312645copy number variation1nstd102humanUncertain significance GRCh37 chr8: 55,370,699-55,372,555 , GRCh38.p12 chr8: 54,458,139-54,459,995 SOX17
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136063copy number variation1nstd213human GRCh37 chr8: 55,310,000-55,500,001 , GRCh38.p12 chr8: 54,397,440-54,587,441 RP1, SOX17, 5 more genes
    nsv6136062copy number variation1nstd213human GRCh37 chr8: 54,950,000-55,810,001 , GRCh38.p12 chr8: 54,037,440-54,897,441 RP1, LYPLA1, 16 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv4683142copy number variation1nstd102humanUncertain significance GRCh37 chr8: 54,978,308-56,436,786 , GRCh38.p12 chr8: 54,065,748-55,524,227 XKR4, LOC105375844, 21 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3919070copy number variation1nstd102humanPathogenic NCBI36 chr8: 54,569,654-58,566,126 , GRCh37.p13 chr8: 54,407,101-58,403,572 , GRCh38.p12 chr8: 53,494,541-57,491,013 BPNT2, RNU6-13P, 73 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 RPL5P22, ARHGEF10, 2105 more genes
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