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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4676210copy number variation1nstd102humanUncertain significance GRCh37 chr20: 4,439,086-4,676,435 , GRCh38.p12 chr20: 4,458,439-4,695,789 PRNP, RPS4XP2, 2 more genes
    nsv3890981copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,092,739-17,091,453 , GRCh38.p12 chr20: 3,112,093-17,110,808 PRNP, LOC107985398, 178 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 PRNP, LRRN4, 129 more genes
    nsv3897192copy number variation1nstd102humanPathogenic GRCh37 chr20: 4,392,930-12,667,768 , GRCh38.p12 chr20: 4,412,283-12,687,121 PRNP, PGAM3P, 102 more genes
    nsv3906854copy number variation1nstd102humanPathogenic GRCh37 chr20: 2,463,101-8,185,680 , GRCh38.p12 chr20: 2,482,455-8,205,033 PRNP, LOC101929098, 121 more genes
    nsv3913207copy number variation1nstd102humanPathogenic GRCh38 chr20: 4,343,033-6,911,730 , GRCh37 chr20: 4,323,680-6,892,377 , NCBI36 chr20: 4,271,680-6,840,377 PRNP, RNA5-8SP7, 45 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 PRNP, TGIF2-RAB5IF, 1314 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 PRNP, LRRN4, 1313 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 PRNP, PKIG, 1311 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 PRNP, COMMD7, 1311 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 PRNP, MIR3646, 1310 more genes
    nsv3908959copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,837-29,638,363 , GRCh38.p12 chr20: 87,196-30,403,687 PRNP, ISM1-AS1, 504 more genes
    nsv3913796copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316 PRNP, RNY4P11, 500 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 PRNP, ISM1-AS1, 498 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 PRNP, LOC105372582, 473 more genes
    nsv3919898copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479 PRNP, MIR3192, 473 more genes
    nsv3907558copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-26,075,841 , GRCh38.p12 chr20: 99,557-26,095,205 PRNP, LINC03086, 469 more genes
    nsv3913704copy number variation1nstd102humanPathogenic GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200 PRNP, NRSN2, 459 more genes
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 PRNP, KRT18P3, 413 more genes
    nsv3921972copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-19,074,923 , GRCh38 chr20: 89,939-19,146,279 , GRCh37 chr20: 70,580-19,126,923 PRNP, PTMAP3, 331 more genes
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