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Items: 1 to 20 of 201

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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
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7071870inversion1nstd229human GRCh38 chr8: 99,825,313-99,969,249 , GRCh37.p13 chr8: 100,837,541-100,981,477 VPS13B, RGS22, 1 more genes
    nsv6637993copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,384-101,278,033 , GRCh38.p12 chr8: 99,779,156-100,265,805 RNF19A, POLR2K, 8 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
    nsv6559151inversion1nstd223human GRCh38 chr8: 99,889,402-99,890,094 , GRCh37.p13 chr8: 100,901,630-100,902,322 COX6C
    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
    nsv6312665copy number variation1nstd102humanUncertain significance GRCh37 chr8: 99,135,566-106,815,766 , GRCh38.p12 chr8: 98,123,338-105,803,538 RNU6-748P, RN7SKP85, 144 more genes
    nsv6277864insertion1nstd214human GRCh38 chr8: 99,876,917-99,876,917 , GRCh37.p13 chr8: 100,889,145-100,889,145 COX6C, VPS13B
    nsv6137320copy number variation1nstd213human GRCh37 chr8: 96,440,000-102,500,001 , GRCh38.p12 chr8: 95,427,772-101,487,773 SDC2, RGS22, 102 more genes
    nsv6136709copy number variation1nstd213human GRCh37 chr8: 94,750,000-101,120,001 , GRCh38.p12 chr8: 93,737,772-100,107,773 SDC2, STK3, 101 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6008939copy number variation1nstd212human GRCh38 chr8: 99,888,300-99,889,824 , GRCh37.p13 chr8: 100,900,528-100,902,052 COX6C
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4676096copy number variation1nstd102humanUncertain significance GRCh37 chr8: 100,791,383-101,278,033 , GRCh38.p12 chr8: 99,779,155-100,265,805 UFM1P3, COX6C, 8 more genes
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