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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148072copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 193,343,827-194,599,635 , GRCh38.p12 chr3: 193,626,038-194,878,906 CPN2, GP5, 36 more genes
    nsv7147284copy number variation1nstd232human GRCh37.p13 chr3: 194,157,944-194,158,038 , GRCh38.p12 chr3: 194,437,215-194,437,309 ATP13A3
    nsv7137945insertion1nstd232human GRCh37.p13 chr3: 194,159,701-194,159,701 , GRCh38.p12 chr3: 194,438,972-194,438,972 ATP13A3
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6733847copy number variation1nstd229human GRCh38 chr3: 194,451,401-194,452,800 , GRCh37.p13 chr3: 194,172,130-194,173,529 ATP13A3
    nsv6733657copy number variation1nstd229human GRCh38 chr3: 194,445,499-194,561,633 , GRCh37.p13 chr3: 194,166,228-194,282,362 RNU6-1101P, RPL23AP93, 2 more genes
    nsv6733575copy number variation1nstd229human GRCh38 chr3: 194,440,401-194,449,000 , GRCh37.p13 chr3: 194,161,130-194,169,729 ATP13A3
    nsv6732659copy number variation1nstd229human GRCh38 chr3: 194,391,019-194,558,345 , GRCh37.p13 chr3: 194,111,748-194,279,074 ATP13A3, ATP13A3-DT, 2 more genes
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6731368copy number variation1nstd229human GRCh38 chr3: 194,478,867-194,487,498 , GRCh37.p13 chr3: 194,199,596-194,208,227 ATP13A3-DT, ATP13A3
    nsv6731295copy number variation1nstd229human GRCh38 chr3: 194,422,912-194,425,810 , GRCh37.p13 chr3: 194,143,641-194,146,539 ATP13A3
    nsv6731265copy number variation1nstd229human GRCh38 chr3: 194,399,894-194,418,737 , GRCh37.p13 chr3: 194,120,623-194,139,466 ATP13A3
    nsv6727962copy number variation1nstd229human GRCh38 chr3: 194,215,451-194,451,362 , GRCh37.p13 chr3: 193,933,240-194,172,091 LRRC15, LINC02036, 6 more genes
    nsv6727467copy number variation1nstd229human GRCh38 chr3: 194,397,482-194,440,381 , GRCh37.p13 chr3: 194,118,211-194,161,110 GP5, ATP13A3
    nsv6726450copy number variation1nstd229human GRCh38 chr3: 194,481,762-194,481,869 , GRCh37.p13 chr3: 194,202,491-194,202,598 ATP13A3
    nsv6721364copy number variation1nstd229human GRCh38 chr3: 194,439,395-194,502,189 , GRCh37.p13 chr3: 194,160,124-194,222,918 ATP13A3-DT, ATP13A3
    nsv6718222copy number variation1nstd229human GRCh38 chr3: 194,179,860-194,436,927 , GRCh37.p13 chr3: 193,897,649-194,157,656 GP5, LINC02048, 6 more genes
    nsv6636634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,396,762-195,009,038 , GRCh38.p12 chr3: 193,678,973-195,288,309 LINC02036, LINC02026, 45 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628551copy number variation1nstd224human GRCh37 chr3: 193,855,650-194,188,614 , GRCh38.p12 chr3: 194,137,861-194,467,885 LINC02036, LOC107986172, 9 more genes
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