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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3137871copy number variation1nstd151human GRCh37 (hg19) chr7: 76,254,836-76,909,975 , GRCh38 (hg38) chr7: 76,625,519-77,280,658 CCDC146, FAM185BP, 20 more genes
    nsv3133749copy number variation1nstd151human GRCh37 (hg19) chr7: 76,240,779-77,016,770 , GRCh38 (hg38) chr7: 76,611,462-77,387,453 CCDC146, GSAP, 22 more genes
    nsv3131416copy number variation1nstd151human GRCh37 (hg19) chr7: 76,916,754-77,026,737 , GRCh38 (hg38) chr7: 77,287,437-77,397,420 CCDC146, LOC107986714, 1 more genes
    nsv3130797copy number variation1nstd151human GRCh37 (hg19) chr7: 76,825,593-76,903,974 , GRCh38 (hg38) chr7: 77,196,276-77,274,657 CCDC146, FGL2, 2 more genes
    nsv3128817copy number variation1nstd151human GRCh37 (hg19) chr7: 76,109,824-76,797,146 , GRCh38 (hg38) chr7: 76,480,507-77,167,829 CCDC146, POMZP3, 20 more genes
    nsv3127574copy number variation3nstd151human GRCh37 (hg19) chr7: 76,922,266-77,035,427 , GRCh38 (hg38) chr7: 77,292,949-77,406,110 CCDC146, GSAP, 1 more genes
    nsv3125441copy number variation1nstd151human GRCh37 (hg19) chr7: 76,885,647-76,991,982 , GRCh38 (hg38) chr7: 77,256,330-77,362,665 CCDC146, LOC102723791, 1 more genes
    nsv3121946copy number variation3nstd151human GRCh37 (hg19) chr7: 76,922,266-77,033,937 , GRCh38 (hg38) chr7: 77,292,949-77,404,620 CCDC146, LOC107986714, 1 more genes
    nsv3121253copy number variation5nstd151human GRCh37 (hg19) chr7: 76,796,983-76,797,146 , GRCh38 (hg38) chr7: 77,167,666-77,167,829 CCDC146
    nsv3119097copy number variation1nstd151human GRCh37 (hg19) chr7: 76,239,527-77,166,967 , GRCh38 (hg38) chr7: 76,610,210-77,537,650 CCDC146, GSAP, 25 more genes
    nsv3089249mobile element insertion1nstd144human GRCh37 (hg19) chr7: 76,778,157-76,778,157 , GRCh38 (hg38) chr7: 77,148,840-77,148,840 CCDC146
    nsv3088972mobile element insertion1nstd144human GRCh37 (hg19) chr7: 76,859,095-76,859,095 , GRCh38 (hg38) chr7: 77,229,778-77,229,778 CCDC146, LOC105375359
    nsv3069778copy number variation1nstd90human GRCh37 (hg19) chr7: 76,870,543-76,870,797 , GRCh38 (hg38) chr7: 77,241,226-77,241,480 CCDC146, LOC105375359
    nsv3060617copy number variation1nstd140human GRCh37 (hg19) chr7: 76,870,543-76,870,797 , GRCh38 (hg38) chr7: 77,241,226-77,241,480 CCDC146, LOC105375359
    nsv3055307copy number variation1nstd140human GRCh38 (hg38) chr7: 77,241,210-77,241,462 , GRCh37 (hg19) chr7: 76,870,527-76,870,779 CCDC146, LOC105375359
    nsv3055306copy number variation1nstd140human GRCh38 (hg38) chr7: 77,241,020-77,241,076 , GRCh37 (hg19) chr7: 76,870,337-76,870,393 CCDC146, LOC105375359
    nsv3055305copy number variation1nstd140human GRCh38 (hg38) chr7: 77,130,629-77,130,921 , GRCh37 (hg19) chr7: 76,759,946-76,760,238 CCDC146
    nsv2817440copy number variation1nstd137human GRCh38 (hg38) chr7: 77,241,227-77,241,480 , GRCh37 (hg19) chr7: 76,870,544-76,870,797 CCDC146, LOC105375359
    esv4003747copy number variation1estd231human GRCh37 (hg19) chr7: 76,870,542-76,870,796 , GRCh38 (hg38) chr7: 77,241,225-77,241,479 CCDC146, LOC105375359
    nsv2777992copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr7: 75,058,408-77,082,896 , GRCh38 (hg38) chr7: 75,429,127-77,453,579 , NCBI36 (hg18) chr7: 74,896,344-76,920,832 CCDC146, HIP1, 52 more genes
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