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Items: 1 to 20 of 194

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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
    nsv7061235inversion1nstd229human GRCh38 chr8: 101,071,242-101,077,977 , GRCh37.p13 chr8: 102,083,470-102,090,205 FLJ42969
    nsv6851626copy number variation1nstd229human GRCh38 chr8: 101,054,108-101,058,779 , GRCh37.p13 chr8: 102,066,336-102,071,007 FLJ42969
    nsv6850944copy number variation1nstd229human GRCh38 chr8: 101,045,640-101,147,217 , GRCh37.p13 chr8: 102,057,868-102,159,445 LOC105375676, LINC03090, 3 more genes
    nsv6847898copy number variation1nstd229human GRCh38 chr8: 101,059,490-101,100,574 , GRCh37.p13 chr8: 102,071,718-102,112,802 FLJ42969
    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
    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
    nsv6313648copy number variation1nstd102humanUncertain significance GRCh37 chr8: 101,532,661-102,444,420 , GRCh38.p12 chr8: 100,520,433-101,432,192 NACA4P, LOC107984005, 29 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
    nsv6308680mobile element insertion1nstd186human GRCh37 chr8: 102,080,287-102,080,338 , GRCh38.p12 chr8: 101,068,059-101,068,110 FLJ42969
    nsv6246400mobile element insertion1nstd215human GRCh38 chr8: 101,063,168-101,063,168 , GRCh37.p13 chr8: 102,075,396-102,075,396 FLJ42969
    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
    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
    nsv6135805copy number variation1nstd213human GRCh37 chr8: 101,190,000-102,670,001 , GRCh38.p12 chr8: 100,177,772-101,657,773 YWHAZ, GRHL2, 37 more genes
    nsv5964491insertion1nstd209human GRCh38 chr8: 101,070,407-101,070,407 , GRCh37.p13 chr8: 102,082,635-102,082,635 FLJ42969
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