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Items: 1 to 20 of 946

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635562copy number variation1nstd227human GRCh37 chr7: 143,425,361-143,437,434 , GRCh38.p12 chr7: 143,728,268-143,740,341 , GRCh38.p12 chr7|NW_018654714.1: 272,587-284,661 TCAF2
    nsv6631783copy number variation1nstd224human GRCh37 chr7: 143,426,263-143,874,190 , GRCh38.p12 chr7: 143,729,170-144,177,097 , GRCh38.p12 chr7|NW_018654714.1: 273,489-589,656 TCAF1, OR2F1, 25 more genes
    nsv6631576copy number variation1nstd224human GRCh37 chr7: 143,429,038-143,870,422 , GRCh38.p12 chr7: 143,731,945-144,173,329 , GRCh38.p12 chr7|NW_018654714.1: 276,264-589,656 TCAF1, OR2A15P, 23 more genes
    nsv6631575copy number variation1nstd224human GRCh37 chr7: 143,117,735-143,141,487 , GRCh38.p12 chr7: 143,420,642-143,444,394 , GRCh38.p12 chr7|NW_018654714.1: 40,006-63,758 TAS2R60, EPHA1-AS1, 1 more genes
    nsv6305054copy number variation1nstd186human GRCh37 chr7: 143,459,445-143,469,897 , GRCh38.p12 chr7|NW_018654714.1: 306,673-317,127 , GRCh38.p12 chr7: 143,762,352-143,772,804 0
    nsv6302801copy number variation1nstd186human GRCh37 chr7: 143,434,993-143,441,897 , GRCh38.p12 chr7|NW_018654714.1: 282,220-289,124 , GRCh38.p12 chr7: 143,737,900-143,744,804 0
    nsv6136969copy number variation1nstd213human GRCh37 chr7: 143,570,000-143,670,001 , GRCh38.p12 chr7: 143,872,907-143,972,908 , GRCh38.p12 chr7|NW_018654714.1: 417,131-517,138 TCAF1, OR2F1, 2 more genes
    nsv6136968copy number variation1nstd213human GRCh37 chr7: 143,560,000-143,920,001 , GRCh38.p12 chr7: 143,862,907-144,222,908 , GRCh38.p12 chr7|NW_018654714.1: 407,132-589,656 TCAF1, OR2A14, 20 more genes
    nsv6135973copy number variation1nstd213human GRCh37 chr7: 143,430,000-143,940,001 , GRCh38.p12 chr7: 143,732,907-144,242,908 , GRCh38.p12 chr7|NW_018654714.1: 277,226-589,656 OR2A15P, TCAF2P1, 29 more genes
    nsv6116675mobile element insertion1nstd186human GRCh37 chr7: 143,153,580-143,153,631 , GRCh38.p12 chr7|NW_018654714.1: 75,851-75,902 , GRCh38.p12 chr7: 143,456,487-143,456,538 EPHA1-AS1
    nsv5387516copy number variation1nstd186human GRCh37 chr7: 143,721,194-143,721,397 , GRCh38.p12 chr7|NW_018654714.1: 568,331-568,534 , GRCh38.p12 chr7: 144,024,101-144,024,304 0
    nsv4827278copy number variation1nstd200human GRCh37 chr7: 143,737,508-143,742,912 , GRCh38.p12 chr7|NW_018654714.1: 584,645-589,657 , GRCh38.p12 chr7: 144,040,415-144,045,819 0
    nsv4827277copy number variation1nstd200human GRCh37 chr7: 143,712,809-143,719,305 , GRCh38.p12 chr7: 144,015,716-144,022,212 , GRCh38.p12 chr7|NW_018654714.1: 559,946-566,442 0
    nsv4827276copy number variation1nstd200human GRCh37 chr7: 143,684,866-143,690,366 , GRCh38.p12 chr7|NW_018654714.1: 532,003-537,503 , GRCh38.p12 chr7: 143,987,773-143,993,273 OR2F1
    nsv4827275copy number variation1nstd200human GRCh37 chr7: 143,637,825-143,638,056 , GRCh38.p12 chr7: 143,940,732-143,940,963 , GRCh38.p12 chr7|NW_018654714.1: 484,960-485,191 OR2F1
    nsv4827274copy number variation1nstd200human GRCh37 chr7: 143,432,840-143,432,956 , GRCh38.p12 chr7|NW_018654714.1: 280,067-280,183 , GRCh38.p12 chr7: 143,735,747-143,735,863 0
    nsv4827273copy number variation1nstd200human GRCh37 chr7: 143,204,809-143,206,693 , GRCh38.p12 chr7: 143,507,716-143,509,600 , GRCh38.p12 chr7|NW_018654714.1: 127,080-128,964 EPHA1-AS1, OR10AC1
    nsv4827272copy number variation1nstd200human GRCh37 chr7: 143,166,295-143,166,387 , GRCh38.p12 chr7: 143,469,202-143,469,294 , GRCh38.p12 chr7|NW_018654714.1: 88,566-88,658 EPHA1-AS1
    nsv4827271copy number variation1nstd200human GRCh37 chr7: 143,154,420-143,184,033 , GRCh38.p12 chr7: 143,457,327-143,486,940 , GRCh38.p12 chr7|NW_018654714.1: 76,691-106,304 OR2R1P, EPHA1-AS1, 1 more genes
    nsv4825402copy number variation1nstd200human GRCh37 chr7: 143,660,195-143,699,177 , GRCh38.p12 chr7: 143,963,102-144,002,084 , GRCh38.p12 chr7|NW_018654714.1: 507,332-546,314 CAPZA1P5, SLC16A1P1, 3 more genes
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