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Items: 1 to 20 of 133

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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
    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
    nsv6845265copy number variation1nstd229human GRCh38 chr8: 47,745,303-48,130,564 , GRCh37.p13 chr8: 48,657,865-49,043,124 UBE2V2-AS1, MCM4, 5 more genes
    nsv6839795copy number variation1nstd229human GRCh38 chr8: 47,978,627-47,979,007 , GRCh37.p13 chr8: 48,891,187-48,891,567 MCM4, RNU6-519P
    nsv6633064copy number variation1nstd224human GRCh37 chr8: 48,691,637-49,066,992 , GRCh38.p12 chr8: 47,779,076-48,154,432 MCM4, PRKDC, 5 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
    nsv6431005copy number variation1nstd223human GRCh38 chr8: 47,967,059-48,023,595 , GRCh37.p13 chr8: 48,879,619-48,936,155 RNU6-519P, UBE2V2, 2 more genes
    nsv6421696copy number variation1nstd223human GRCh38 chr8: 47,978,496-47,983,681 , GRCh37.p13 chr8: 48,891,056-48,896,241 RNU6-519P, MCM4
    nsv6419939copy number variation1nstd223human GRCh38 chr8: 47,978,362-47,979,706 , GRCh37.p13 chr8: 48,890,922-48,892,266 RNU6-519P, MCM4
    nsv6312916copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,734-49,833,824 , GRCh38.p12 chr8: 47,774,173-48,921,265 LOC107986942, UBE2V2, 21 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
    nsv5476390copy number variation1nstd206human GRCh38 chr8: 47,978,450-47,983,713 , GRCh37.p13 chr8: 48,891,010-48,896,273 RNU6-519P, MCM4
    nsv4965243copy number variation1nstd200human GRCh38 chr8: 47,978,278-47,979,685 , GRCh37.p13 chr8: 48,890,838-48,892,245 MCM4, RNU6-519P
    nsv4825806copy number variation1nstd200human GRCh37 chr8: 48,890,832-48,892,251 , GRCh38.p12 chr8: 47,978,272-47,979,691 RNU6-519P, MCM4
    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
    nsv4714389copy number variation1nstd195human GRCh38.p12 chr8: 47,945,691-48,148,991 , GRCh37 chr8: 48,858,251-49,061,551 MCM4, PRKDC, 4 more genes
    nsv4670003copy number variation1nstd186human GRCh37 chr8: 48,892,501-48,896,700 , GRCh38.p12 chr8: 47,979,941-47,984,140 RNU6-519P
    nsv4616474copy number variation1nstd183human GRCh37 chr8: 48,842,234-48,964,415 , GRCh38.p12 chr8: 47,929,674-48,051,855 MCM4, PRKDC, 4 more genes
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