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Items: 1 to 20 of 262

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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
    nsv7062607inversion1nstd229human GRCh38 chr8: 103,381,760-103,384,227 , GRCh37.p13 chr8: 104,393,988-104,396,455 RNU6-1011P, CTHRC1
    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
    nsv6851891copy number variation1nstd229human GRCh38 chr8: 103,354,601-103,427,300 , GRCh37.p13 chr8: 104,366,829-104,439,528 DCAF13, CTHRC1, 2 more genes
    nsv6850483copy number variation1nstd229human GRCh38 chr8: 103,377,646-103,379,460 , GRCh37.p13 chr8: 104,389,874-104,391,688 CTHRC1
    nsv6848843copy number variation1nstd229human GRCh38 chr8: 103,370,701-103,371,000 , GRCh37.p13 chr8: 104,382,929-104,383,228 CTHRC1
    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
    nsv6843518copy number variation1nstd229human GRCh38 chr8: 103,349,875-103,866,372 , GRCh37.p13 chr8: 104,362,103-104,878,600 PTMAP15, TARBP2P1, 8 more genes
    nsv6637517copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,370,102-104,770,147 , GRCh38.p12 chr8: 103,357,874-103,757,919 SLC25A32, LOC101101841, 7 more genes
    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
    nsv6422162copy number variation1nstd223human GRCh38 chr8: 103,349,875-103,866,372 , GRCh37.p13 chr8: 104,362,103-104,878,600 CTHRC1, RPS6P9, 8 more genes
    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
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
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