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Items: 1 to 20 of 836

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145856copy number variation1nstd232human GRCh37.p13 chr19: 40,480,344-40,480,426 , GRCh38.p12 chr19: 39,974,437-39,974,519 , GRCh38.p12 chr19|NW_009646206.1: 249,580-249,662 PSMC4
    nsv7145190copy number variation1nstd232human GRCh37.p13 chr19: 40,480,537-40,480,637 , GRCh38.p12 chr19: 39,974,630-39,974,730 , GRCh38.p12 chr19|NW_009646206.1: 249,773-249,873 PSMC4
    nsv7144323copy number variation1nstd232human GRCh37.p13 chr19: 40,325,201-40,325,305 , GRCh38.p12 chr19: 39,834,561-39,834,665 , GRCh38.p12 chr19|NW_009646206.1: 94,437-94,541 FBL, DYRK1B
    nsv7138598copy number variation1nstd232human GRCh37.p13 chr19: 40,330,964-40,331,049 , GRCh38.p12 chr19: 39,840,324-39,840,409 , GRCh38.p12 chr19|NW_009646206.1: 100,200-100,285 FBL
    nsv7137666copy number variation1nstd232human GRCh37.p13 chr19: 40,485,890-40,485,974 , GRCh38.p12 chr19: 39,979,983-39,980,067 , GRCh38.p12 chr19|NW_009646206.1: 255,126-255,210 PSMC4
    nsv6306035copy number variation1nstd186human GRCh37 chr19: 40,365,514-40,370,840 , GRCh38.p12 chr19: 39,874,874-39,880,200 , GRCh38.p12 chr19|NW_009646206.1: 134,750-140,076 FCGBP
    nsv6133702copy number variation1nstd213human GRCh37 chr19: 40,470,000-40,680,001 , GRCh38.p12 chr19: 39,964,093-40,174,094 , GRCh38.p12 chr19|NW_009646206.1: 239,236-370,917 PSMC4, ZNF780B, 4 more genes
    nsv6127770copy number variation1nstd186human GRCh37 chr19: 40,257,560-40,257,850 , GRCh38.p12 chr19: 39,766,920-39,767,210 , GRCh38.p12 chr19|NW_009646206.1: 26,796-27,086 0
    nsv6124785copy number variation1nstd186human GRCh37 chr19: 40,464,003-40,464,881 , GRCh38.p12 chr19: 39,958,096-39,958,974 , GRCh38.p12 chr19|NW_009646206.1: 233,239-234,117 0
    nsv6124193copy number variation1nstd186human GRCh37 chr19: 40,404,708-40,405,219 , GRCh38.p12 chr19|NW_009646206.1: 173,944-174,455 FCGBP
    nsv6116699copy number variation1nstd186human GRCh37 chr19: 40,368,065-40,384,320 , GRCh38.p12 chr19|NW_009646206.1: 137,301-153,556 , GRCh38.p12 chr19: 39,877,425-39,893,680 FCGBP
    nsv6116098copy number variation1nstd186human GRCh37 chr19: 40,384,640-40,405,767 , GRCh38.p12 chr19|NW_009646206.1: 157,796-175,003 FCGBP
    nsv5384089mobile element deletion2nstd186human GRCh37 chr19: 40,257,560-40,257,850 , GRCh38.p12 chr19|NW_009646206.1: 26,796-27,086 , GRCh38.p12 chr19: 39,766,920-39,767,210 0
    nsv5345226translocation1nstd200human GRCh37 chr19: 40,509,429-40,509,429 , GRCh37 chr19: 40,507,028-40,507,028 , GRCh38.p12 chr19: 40,001,121-40,001,121 , GRCh38.p12 chr19: 40,003,522-40,003,522 , GRCh38.p12 chr19|NW_009646206.1: 276,264-276,264 , GRCh38.p12 chr19|NW_009646206.1: 278,665-278,665 ZNF546
    nsv5341725translocation1nstd200human GRCh37 chr11: 35,984,970-35,984,970 , GRCh37 chr19: 40,249,151-40,249,151 , GRCh38.p12 chr19|NW_009646206.1: 18,387-18,387 , GRCh38.p12 chr11: 35,963,420-35,963,420 , GRCh38.p12 chr19: 39,758,511-39,758,511 LDLRAD3
    nsv5340352translocation1nstd200human GRCh37 chr19: 40,263,731-40,263,731 , GRCh37 chr19: 40,265,002-40,265,002 , GRCh38.p12 chr19: 39,773,091-39,773,091 , GRCh38.p12 chr19|NW_009646206.1: 34,238-34,238 , GRCh38.p12 chr19: 39,774,362-39,774,362 , GRCh38.p12 chr19|NW_009646206.1: 32,967-32,967 0
    nsv5333581translocation1nstd200human GRCh37 chr19: 40,515,703-40,515,703 , GRCh37 chr19: 40,515,917-40,515,917 , GRCh38.p12 chr19: 40,010,010-40,010,010 , GRCh38.p12 chr19: 40,009,796-40,009,796 , GRCh38.p12 chr19|NW_009646206.1: 284,939-284,939 , GRCh38.p12 chr19|NW_009646206.1: 285,153-285,153 ZNF546
    nsv5333417translocation1nstd200human GRCh37 chr19: 40,566,970-40,566,970 , GRCh37 chr19: 40,567,063-40,567,063 , GRCh38.p12 chr19|NW_009646206.1: 336,206-336,206 , GRCh38.p12 chr19: 40,061,156-40,061,156 , GRCh38.p12 chr19: 40,061,063-40,061,063 , GRCh38.p12 chr19|NW_009646206.1: 336,299-336,299 ZNF780B
    nsv4868360copy number variation1nstd200human GRCh37 chr19: 40,580,595-40,581,708 , GRCh38.p12 chr19|NW_009646206.1: 349,831-350,944 , GRCh38.p12 chr19: 40,074,688-40,075,801 ZNF780A
    nsv4868359copy number variation1nstd200human GRCh37 chr19: 40,525,309-40,525,488 , GRCh38.p12 chr19: 40,019,402-40,019,581 , GRCh38.p12 chr19|NW_009646206.1: 294,545-294,724 ZNF546
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