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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7056463inversion1nstd229human GRCh38 chr1: 20,697,162-20,724,257 , GRCh37.p13 chr1: 21,023,655-21,050,750 KIF17, SH2D5
    nsv7055295inversion1nstd229human GRCh38 chr1: 20,526,331-21,860,622 , GRCh37.p13 chr1: 20,852,824-22,187,115 USP48, ECE1, 31 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7049047inversion1nstd229human GRCh38 chr1: 20,644,333-20,775,008 , GRCh37.p13 chr1: 20,970,826-21,101,501 PINK1, DDOST, 4 more genes
    nsv7047315inversion1nstd229human GRCh38 chr1: 20,715,212-20,790,995 , GRCh37.p13 chr1: 21,041,705-21,117,488 HP1BP3, KIF17, 1 more genes
    nsv6647225copy number variation1nstd229human GRCh38 chr1: 20,718,001-20,724,400 , GRCh37.p13 chr1: 21,044,494-21,050,893 KIF17, SH2D5
    nsv6647223copy number variation1nstd229human GRCh38 chr1: 20,707,675-20,727,337 , GRCh37.p13 chr1: 21,034,168-21,053,830 KIF17, SH2D5
    nsv6647222copy number variation1nstd229human GRCh38 chr1: 20,705,306-20,735,524 , GRCh37.p13 chr1: 21,031,799-21,062,017 KIF17, SH2D5
    nsv6647160copy number variation1nstd229human GRCh38 chr1: 20,691,401-20,733,600 , GRCh37.p13 chr1: 21,017,894-21,060,093 SH2D5, KIF17
    nsv6647159copy number variation1nstd229human GRCh38 chr1: 20,681,355-20,717,994 , GRCh37.p13 chr1: 21,007,848-21,044,487 KIF17, SH2D5
    nsv6647086copy number variation1nstd229human GRCh38 chr1: 20,707,045-20,718,045 , GRCh37.p13 chr1: 21,033,538-21,044,538 SH2D5, KIF17
    nsv6646707copy number variation1nstd229human GRCh38 chr1: 20,701,613-20,721,441 , GRCh37.p13 chr1: 21,028,106-21,047,934 KIF17, SH2D5
    nsv6646702copy number variation1nstd229human GRCh38 chr1: 20,609,201-20,761,400 , GRCh37.p13 chr1: 20,935,694-21,087,893 CDA, PINK1-AS, 6 more genes
    nsv6542533inversion1nstd223human GRCh38 chr1: 20,715,209-20,790,995 , GRCh37.p13 chr1: 21,041,702-21,117,488 HP1BP3, KIF17, 1 more genes
    nsv6331693copy number variation1nstd223human GRCh38 chr1: 20,707,675-20,727,332 , GRCh37.p13 chr1: 21,034,168-21,053,825 KIF17, SH2D5
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
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