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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7098191copy number variation1nstd102humanUncertain significance GRCh37 chr9: 107,546,596-108,536,361 , GRCh38.p12 chr9: 104,784,315-105,774,080 TMEM38B, CT70, 14 more genes
    nsv7097917copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,358,859-108,484,922 , GRCh38.p12 chr9: 105,596,578-105,722,641 FKTN, TAL2, 3 more genes
    nsv7075258inversion1nstd229human GRCh38 chr9: 105,659,939-106,272,714 , GRCh37.p13 chr9: 108,422,220-109,034,995 LOC107987107, TMEM38B, 6 more genes
    nsv7071806inversion1nstd229human GRCh38 chr9: 105,659,830-105,919,918 , GRCh37.p13 chr9: 108,422,111-108,682,199 DEPDC1P2, TAL2, 4 more genes
    nsv7062784inversion1nstd229human GRCh38 chr9: 105,247,017-105,897,262 , GRCh37.p13 chr9: 108,009,298-108,659,543 SLC44A1, RALGAPA1P1, 9 more genes
    nsv7058700inversion1nstd229human GRCh38 chr9: 105,563,937-105,790,249 , GRCh37.p13 chr9: 108,326,218-108,552,530 DEPDC1P2, LOC100421293, 4 more genes
    nsv6865426copy number variation1nstd229human GRCh38 chr9: 105,630,787-105,698,163 , GRCh37.p13 chr9: 108,393,068-108,460,444 TAL2, TMEM38B, 1 more genes
    nsv6858749copy number variation1nstd229human GRCh38 chr9: 105,632,543-105,844,896 , GRCh37.p13 chr9: 108,394,824-108,607,177 LOC107987107, TMEM38B, 4 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6564558inversion1nstd223human GRCh38 chr9: 105,545,205-105,764,347 , GRCh37.p13 chr9: 108,307,486-108,526,628 FKTN, TAL2, 6 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6312934copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,337,314-108,468,054 , GRCh38.p12 chr9: 105,575,033-105,705,773 FKTN, TMEM38B, 2 more genes
    nsv6312744copy number variation2nstd102humanUncertain significance GRCh37 chr9: 108,358,859-108,510,491 , GRCh38.p12 chr9: 105,596,578-105,748,210 TAL2, FKTN, 3 more genes
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6136630copy number variation1nstd213human GRCh37 chr9: 108,290,000-109,010,001 , GRCh38.p12 chr9: 105,527,719-106,247,720 TMEM38B, DEPDC1P2, 10 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4974796copy number variation1nstd200human GRCh38 chr9: 105,590,424-105,692,256 , GRCh37.p13 chr9: 108,352,705-108,454,537 TAL2, FKTN
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