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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6854742copy number variation1nstd229human GRCh38 chr8: 47,691,701-47,743,048 , GRCh37.p13 chr8: 48,604,263-48,655,610 SPIDR, CEBPD
    nsv6852681copy number variation1nstd229human GRCh38 chr8: 47,716,464-47,892,923 , GRCh37.p13 chr8: 48,629,026-48,805,484 CEBPD, SPIDR, 1 more genes
    nsv6851281copy number variation1nstd229human GRCh38 chr8: 47,687,801-47,737,400 , GRCh37.p13 chr8: 48,600,363-48,649,962 SPIDR, CEBPD
    nsv6850722copy number variation1nstd229human GRCh38 chr8: 47,597,201-48,026,222 , GRCh37.p13 chr8: 48,509,763-48,938,782 CEBPD, RNU6-519P, 7 more genes
    nsv6847659copy number variation1nstd229human GRCh38 chr8: 47,666,938-47,817,720 , GRCh37.p13 chr8: 48,579,500-48,730,281 PRKDC, CEBPD, 2 more genes
    nsv6840774copy number variation1nstd229human GRCh38 chr8: 47,610,610-47,761,886 , GRCh37.p13 chr8: 48,523,172-48,674,448 CEBPD, SPIDR, 1 more genes
    nsv6569657inversion1nstd223human GRCh38 chr8: 47,319,822-52,044,550 , GRCh37.p13 chr8: 48,405,007-52,957,110 UBE2V2-AS1, BRIX1P1, 48 more genes
    nsv6434617copy number variation1nstd223human GRCh38 chr8: 47,710,545-47,907,837 , GRCh37.p13 chr8: 48,623,107-48,820,397 CEBPD, SPIDR, 1 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6290721copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,336,764-48,752,512 , GRCh38.p12 chr8: 47,424,202-47,839,951 PRKDC, SPIDR, 5 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136052copy number variation1nstd213human GRCh37 chr8: 48,380,000-49,290,001 , GRCh38.p12 chr8: 47,467,438-48,377,441 CEBPD, MCM4, 17 more genes
    nsv4965239copy number variation1nstd200human GRCh38 chr8: 47,729,737-47,747,273 , GRCh37.p13 chr8: 48,642,299-48,659,835 CEBPD, SPIDR
    nsv4965238copy number variation1nstd200human GRCh38 chr8: 47,698,530-47,790,714 , GRCh37.p13 chr8: 48,611,092-48,703,275 SPIDR, PRKDC, 1 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4710617copy number variation1nstd195human GRCh37 chr8: 48,539,951-48,664,601 , GRCh38.p12 chr8: 47,627,389-47,752,039 CEBPD, SPIDR, 1 more genes
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
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