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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7077334inversion1nstd229human GRCh38 chr8: 102,796,562-104,427,483 , GRCh37.p13 chr8: 103,808,790-105,439,711 DCSTAMP, LOC107984007, 33 more genes
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7072980inversion1nstd229human GRCh38 chr8: 102,790,775-104,428,155 , GRCh37.p13 chr8: 103,803,003-105,440,383 DCSTAMP, ATP6V1C1, 33 more genes
    nsv7071528inversion1nstd229human GRCh38 chr8: 103,103,016-104,690,333 , GRCh37.p13 chr8: 104,115,244-105,702,561 LOC105375690, DCAF13, 27 more genes
    nsv6858085copy number variation1nstd229human GRCh38 chr8: 103,174,080-103,349,054 , GRCh37.p13 chr8: 104,186,308-104,361,282 SNORD173, FZD6, 2 more genes
    nsv6856867copy number variation1nstd229human GRCh38 chr8: 103,290,214-103,958,039 , GRCh37.p13 chr8: 104,302,442-104,970,267 SNORD173, FZD6, 12 more genes
    nsv6851448copy number variation1nstd229human GRCh38 chr8: 103,071,801-103,331,000 , GRCh37.p13 chr8: 104,084,029-104,343,228 MTND1P5, BAALC-AS1, 11 more genes
    nsv6851163copy number variation1nstd229human GRCh38 chr8: 103,298,730-103,325,029 , GRCh37.p13 chr8: 104,310,958-104,337,257 LOC105369147, FZD6, 1 more genes
    nsv6849485copy number variation1nstd229human GRCh38 chr8: 103,324,201-103,329,600 , GRCh37.p13 chr8: 104,336,429-104,341,828 FZD6
    nsv6845547copy number variation1nstd229human GRCh38 chr8: 103,189,601-103,384,200 , GRCh37.p13 chr8: 104,201,829-104,396,428 SNORD173, CTHRC1, 4 more genes
    nsv6841878copy number variation1nstd229human GRCh38 chr8: 103,302,401-103,310,500 , GRCh37.p13 chr8: 104,314,629-104,322,728 SNORD173, FZD6
    nsv6838809copy number variation1nstd229human GRCh38 chr8: 103,295,365-103,301,680 , GRCh37.p13 chr8: 104,307,593-104,313,908 FZD6, LOC105369147
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6432858copy number variation1nstd223human GRCh38 chr8: 103,314,337-103,315,095 , GRCh37.p13 chr8: 104,326,565-104,327,323 FZD6
    nsv6431859copy number variation1nstd223human GRCh38 chr8: 103,298,301-103,299,700 , GRCh37.p13 chr8: 104,310,529-104,311,928 FZD6, LOC105369147
    nsv6425483copy number variation1nstd223human GRCh38 chr8: 103,292,301-103,303,200 , GRCh37.p13 chr8: 104,304,529-104,315,428 FZD6, LOC105369147
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
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