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Items: 1 to 20 of 962

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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
    nsv7146447copy number variation1nstd232human GRCh37.p13 chr8: 51,647,360-51,647,409 , GRCh38.p12 chr8: 50,734,800-50,734,849 SNTG1
    nsv7143066insertion1nstd232human GRCh37.p13 chr8: 51,482,802-51,482,802 , GRCh38.p12 chr8: 50,570,242-50,570,242 SNTG1
    nsv7077350inversion1nstd229human GRCh38 chr8: 50,515,276-50,515,981 , GRCh37.p13 chr8: 51,427,836-51,428,541 SNTG1
    nsv7076924inversion1nstd229human GRCh38 chr8: 49,925,764-49,925,869 , GRCh37.p13 chr8: 50,838,324-50,838,429 SNTG1
    nsv7074442inversion1nstd229human GRCh38 chr8: 50,777,685-50,777,717 , GRCh37.p13 chr8: 51,690,245-51,690,277 SNTG1
    nsv7074333inversion1nstd229human GRCh38 chr8: 50,582,417-50,582,509 , GRCh37.p13 chr8: 51,494,977-51,495,069 SNTG1
    nsv7074141inversion1nstd229human GRCh38 chr8: 48,828,025-51,794,653 , GRCh37.p13 chr8: 49,740,584-52,707,213 CYCSP22, LOC100422267, 19 more genes
    nsv7070965inversion1nstd229human GRCh38 chr8: 50,686,510-50,686,572 , GRCh37.p13 chr8: 51,599,070-51,599,132 SNTG1
    nsv7070702inversion1nstd229human GRCh38 chr8: 50,733,513-50,802,372 , GRCh37.p13 chr8: 51,646,073-51,714,932 SNTG1, CYCSP22
    nsv7069868inversion1nstd229human GRCh38 chr8: 50,140,515-50,147,439 , GRCh37.p13 chr8: 51,053,075-51,059,999 SNTG1
    nsv7068366inversion1nstd229human GRCh38 chr8: 50,115,044-50,125,479 , GRCh37.p13 chr8: 51,027,604-51,038,039 SNTG1
    nsv7067293inversion1nstd229human GRCh38 chr8: 50,670,339-50,917,817 , GRCh37.p13 chr8: 51,582,899-51,830,377 SNTG1, CYCSP22, 1 more genes
    nsv7065573inversion1nstd229human GRCh38 chr8: 50,010,746-51,804,722 , GRCh37.p13 chr8: 50,923,306-52,717,282 LOC105375830, LOC100422267, 10 more genes
    nsv7064222inversion1nstd229human GRCh38 chr8: 50,077,499-50,150,301 , GRCh37.p13 chr8: 50,990,059-51,062,861 SNTG1
    nsv7061671inversion1nstd229human GRCh38 chr8: 50,018,535-50,319,049 , GRCh37.p13 chr8: 50,931,095-51,231,609 LOC105375829, SNTG1
    nsv7060780inversion1nstd229human GRCh38 chr8: 50,146,883-50,166,810 , GRCh37.p13 chr8: 51,059,443-51,079,370 SNTG1
    nsv6858053copy number variation1nstd229human GRCh38 chr8: 50,229,621-50,242,707 , GRCh37.p13 chr8: 51,142,181-51,155,267 SNTG1, LOC105375829
    nsv6858044copy number variation1nstd229human GRCh38 chr8: 50,312,425-50,315,758 , GRCh37.p13 chr8: 51,224,985-51,228,318 SNTG1
    nsv6857980copy number variation1nstd229human GRCh38 chr8: 50,118,533-50,125,732 , GRCh37.p13 chr8: 51,031,093-51,038,292 SNTG1
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