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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv7039656inversion1nstd229human GRCh38 chr7: 75,704,904-77,508,509 , GRCh37.p13 chr7: 75,921,853-77,137,826 HSPB1, FAM185BP, 45 more genes
    nsv6836985copy number variation1nstd229human GRCh38 chr7: 77,241,938-77,367,747 , GRCh37.p13 chr7: 76,871,255-76,997,064 GSAP, LOC102723791, 2 more genes
    nsv6836675copy number variation1nstd229human GRCh38 chr7: 77,317,982-77,449,580 , GRCh37.p13 chr7: 76,947,299-77,078,897 GSAP, LOC101927243
    nsv6835499copy number variation1nstd229human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, PTPN12, 2 more genes
    nsv6829277copy number variation1nstd229human GRCh38 chr7: 77,400,769-77,408,426 , GRCh37.p13 chr7: 77,030,086-77,037,743 GSAP
    nsv6828876copy number variation1nstd229human GRCh38 chr7: 77,338,871-77,341,474 , GRCh37.p13 chr7: 76,968,188-76,970,791 GSAP
    nsv6826989copy number variation1nstd229human GRCh38 chr7: 77,272,601-77,320,200 , GRCh37.p13 chr7: 76,901,918-76,949,517 LOC102723791, GSAP, 1 more genes
    nsv6824220copy number variation1nstd229human GRCh38 chr7: 77,385,524-77,385,688 , GRCh37.p13 chr7: 77,014,841-77,015,005 GSAP
    nsv6823171copy number variation1nstd229human GRCh38 chr7: 77,310,172-77,310,396 , GRCh37.p13 chr7: 76,939,489-76,939,713 GSAP
    nsv6820495copy number variation1nstd229human GRCh38 chr7: 77,397,894-77,399,903 , GRCh37.p13 chr7: 77,027,211-77,029,220 GSAP
    nsv6818853copy number variation1nstd229human GRCh38 chr7: 77,374,901-77,378,600 , GRCh37.p13 chr7: 77,004,218-77,007,917 GSAP
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6617704copy number variation1nstd223human GRCh38 chr7: 77,392,183-77,392,509 , GRCh37.p13 chr7: 77,021,500-77,021,826 GSAP
    nsv6615708copy number variation1nstd223human GRCh38 chr7: 77,345,101-77,620,000 , GRCh37.p13 chr7: 76,974,418-77,249,317 GCNT1P5, LOC101927243, 2 more genes
    nsv6609612copy number variation1nstd223human GRCh38 chr7: 77,409,901-77,420,400 , GRCh37.p13 chr7: 77,039,218-77,049,717 LOC101927243, GSAP
    nsv6608583copy number variation1nstd223human GRCh38 chr7: 77,385,293-77,498,748 , GRCh37.p13 chr7: 77,014,610-77,128,065 GCNT1P5, GSAP, 1 more genes
    nsv6601603copy number variation1nstd223human GRCh38 chr7: 77,355,990-77,356,070 , GRCh37.p13 chr7: 76,985,307-76,985,387 GSAP
    nsv6572498inversion1nstd223human GRCh38 chr7: 75,704,918-77,511,682 , GRCh37.p13 chr7: 75,921,853-77,140,999 LOC645324, FDPSP2, 45 more genes
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