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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098477copy number variation1nstd102humanPathogenic GRCh37 chr9: 94,485,944-95,527,026 , GRCh38.p12 chr9: 91,723,662-92,764,744 LINC00475, MTATP6P29, 30 more genes
    nsv6870540copy number variation1nstd229human GRCh38 chr9: 92,668,035-92,671,850 , GRCh37.p13 chr9: 95,430,317-95,434,132 LOC107987095, IPPK
    nsv6869082copy number variation1nstd229human GRCh38 chr9: 92,624,718-92,624,750 , GRCh37.p13 chr9: 95,387,000-95,387,032 IPPK
    nsv6864586copy number variation1nstd229human GRCh38 chr9: 92,616,014-92,616,211 , GRCh37.p13 chr9: 95,378,296-95,378,493 LOC100128361, CENPP, 1 more genes
    nsv6859741copy number variation1nstd229human GRCh38 chr9: 92,599,301-92,808,400 , GRCh37.p13 chr9: 95,361,583-95,570,682 ANKRD19P, LOC101929748, 6 more genes
    nsv6637423copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,079,794-95,503,060 , GRCh38.p12 chr9: 92,317,512-92,740,778 IPPK, LOC100420779, 11 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
    nsv6633497copy number variation1nstd224human GRCh37 chr9: 94,927,564-95,560,534 , GRCh38.p12 chr9: 92,165,282-92,798,252 IPPK, IARS1, 17 more genes
    nsv6556848inversion1nstd223human GRCh38 chr9: 90,743,255-92,932,434 , GRCh37.p13 chr9: 93,505,537-95,694,716 MIR3651, IARS1, 54 more genes
    nsv6451836copy number variation1nstd223human GRCh38 chr9: 92,617,509-92,617,562 , GRCh37.p13 chr9: 95,379,791-95,379,844 CENPP, IPPK, 1 more genes
    nsv6447123copy number variation1nstd223human GRCh38 chr9: 92,668,122-92,678,809 , GRCh37.p13 chr9: 95,430,404-95,441,091 LOC107987095, RPL21P86, 1 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
    nsv6315179copy number variation1nstd102humanPathogenic GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300 SUGT1P4-STRA6LP, NR4A3, 255 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
    nsv6313293copy number variation2nstd102humanUncertain significance GRCh37 chr9: 94,794,747-95,527,026 , GRCh38.p12 chr9: 92,032,465-92,764,744 SNORA84, IARS1, 25 more genes
    nsv6291371copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,052,447-95,382,122 , GRCh38.p12 chr9: 92,290,165-92,619,840 ASPN, NOL8, 11 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6257908mobile element insertion1nstd215human GRCh38 chr9: 92,669,912-92,669,912 , GRCh37.p13 chr9: 95,432,194-95,432,194 LOC107987095, IPPK
    nsv6136399copy number variation1nstd213human GRCh37 chr9: 94,540,000-95,630,001 , GRCh38.p12 chr9: 91,777,718-92,867,719 ECM2, ROR2, 36 more genes
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