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Items: 1 to 20 of 236

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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
    nsv6876865copy number variation1nstd229human GRCh38 chr9: 92,527,737-92,527,779 , GRCh37.p13 chr9: 95,290,019-95,290,061 MIR4670, ECM2, 1 more genes
    nsv6871993copy number variation1nstd229human GRCh38 chr9: 92,364,249-92,536,252 , GRCh37.p13 chr9: 95,126,531-95,298,534 ECM2, OGN, 4 more genes
    nsv6870568copy number variation1nstd229human GRCh38 chr9: 92,503,530-92,503,711 , GRCh37.p13 chr9: 95,265,812-95,265,993 CENPP, ECM2
    nsv6870487copy number variation1nstd229human GRCh38 chr9: 91,906,361-92,583,443 , GRCh37.p13 chr9: 94,668,643-95,345,725 ROR2, LOC100420779, 25 more genes
    nsv6860500copy number variation1nstd229human GRCh38 chr9: 92,520,001-92,542,400 , GRCh37.p13 chr9: 95,282,283-95,304,682 CENPP, MIR4670, 1 more genes
    nsv6638032copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,076,710-95,263,214 , GRCh38.p12 chr9: 92,314,428-92,500,932 OMD, CENPP, 5 more genes
    nsv6637685copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,666,958-95,339,157 , GRCh38.p12 chr9: 91,904,676-92,576,875 ECM2, IARS1, 25 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
    nsv6567863inversion1nstd223human GRCh38 chr9: 92,531,853-92,532,262 , GRCh37.p13 chr9: 95,294,135-95,294,544 ECM2, CENPP
    nsv6558380inversion1nstd223human GRCh38 chr9: 92,537,142-92,537,542 , GRCh37.p13 chr9: 95,299,424-95,299,824 ECM2, CENPP
    nsv6556848inversion1nstd223human GRCh38 chr9: 90,743,255-92,932,434 , GRCh37.p13 chr9: 93,505,537-95,694,716 MIR3651, IARS1, 54 more genes
    nsv6440412copy number variation1nstd223human GRCh38 chr9: 92,520,061-92,607,532 , GRCh37.p13 chr9: 95,282,343-95,369,814 MIR4670, ECM2, 1 more genes
    nsv6436927copy number variation1nstd223human GRCh38 chr9: 92,518,037-92,519,281 , GRCh37.p13 chr9: 95,280,319-95,281,563 CENPP, ECM2
    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
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