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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7016786copy number variation1nstd229human GRCh38 chr19: 10,281,401-10,455,600 , GRCh37.p13 chr19: 10,392,077-10,566,276 FDX2, PDE4A, 9 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6624627copy number variation1nstd224human GRCh37 chr19: 10,387,268-10,415,648 , GRCh38.p12 chr19: 10,276,592-10,304,972 ICAM5, ICAM1, 2 more genes
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6144509copy number variation1nstd206human GRCh38 chr19: 10,276,000-10,294,000 , GRCh37.p13 chr19: 10,386,676-10,404,676 ICAM1, ICAM4, 1 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5932401copy number variation1nstd209human GRCh38 chr19: 10,287,131-10,287,235 , GRCh37.p13 chr19: 10,397,807-10,397,911 ICAM4
    nsv5288069copy number variation1nstd204human GRCh38.p13 chr19: 10,216,408-10,327,822 , GRCh37.p13 chr19: 10,327,084-10,438,498 FDX2, MRPL4, 9 more genes
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5179364mobile element insertion1nstd203human GRCh38 chr19: 10,288,258-10,288,284 , GRCh37.p13 chr19: 10,398,934-10,398,960 ICAM4, ICAM5
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 more genes
    nsv3920643copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688 MIR4748, ZGLP1, 36 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
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