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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884539copy number variation1nstd102humanPathogenic GRCh37 chr1: 8,018,845-8,044,954 , GRCh38.p12 chr1: 7,958,785-7,984,894 PARK7
    nsv7095540copy number variation1nstd102humanPathogenic GRCh37 chr1: 8,022,846-8,037,818 , GRCh38.p12 chr1: 7,962,786-7,977,758 PARK7
    nsv3871900copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 8,029,385-8,029,484 , GRCh38 chr1: 7,969,325-7,969,424 PARK7
    nsv3888788copy number variation1nstd102humanBenign GRCh37 chr1: 8,020,162-8,022,197 , GRCh38.p12 chr1: 7,960,102-7,962,137 PARK7
    nsv4455033copy number variation1nstd102humanUncertain significance GRCh38 chr1: 7,962,776-7,970,975 , GRCh37 chr1: 8,022,836-8,031,035 PARK7
    nsv5673413copy number variation1nstd102humanPathogenic GRCh37 chr1: 7,995,073-8,031,023 , GRCh38.p12 chr1: 7,935,013-7,970,963 PARK7, TNFRSF9
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 PARK7, RPL9P11, 466 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 PARK7, LOC107985467, 386 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 PARK7, MFFP1, 364 more genes
    nsv3873030copy number variation1nstd102humanPathogenic GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663 PARK7, RN7SL451P, 376 more genes
    nsv3900236copy number variation1nstd102humanPathogenic GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383 PARK7, PDPN, 333 more genes
    nsv3888433copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316 PARK7, AURKAIP1, 356 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 PARK7, GPR157, 313 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 PARK7, RNF223, 325 more genes
    nsv3899046copy number variation1nstd102humanPathogenic GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775 PARK7, PRKCZ-DT, 315 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 PARK7, VWA1, 311 more genes
    nsv3905483copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588 PARK7, VPS13D, 240 more genes
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 PARK7, VAMP3, 245 more genes
    nsv4436631copy number variation1nstd102humanPathogenic GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784 PARK7, LINC02606, 253 more genes
    nsv3913374copy number variation1nstd102humanPathogenic NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327 PARK7, LOC105378593, 252 more genes
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