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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6948033copy number variation1nstd229human GRCh38 chr13: 52,999,900-53,132,152 , GRCh37.p13 chr13: 53,574,035-53,706,287 OLFM4, LINC01065
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6483726copy number variation1nstd223human GRCh38 chr13: 53,050,981-53,051,361 , GRCh37.p13 chr13: 53,625,116-53,625,496 OLFM4
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6133100copy number variation1nstd213human GRCh37 chr13: 52,550,000-56,590,001 , GRCh38.p12 chr13: 51,975,864-56,015,867 ATP7B, NEK3, 34 more genes
    nsv6132654copy number variation1nstd213human GRCh37 chr13: 53,570,000-53,940,001 , GRCh38.p12 chr13: 52,995,865-53,365,866 OLFM4, PCDH8P1, 2 more genes
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6129356insertion1nstd186human GRCh37 chr13: 53,608,121-53,608,135 , GRCh38.p12 chr13: 53,033,986-53,034,000 OLFM4
    nsv5972679insertion1nstd209human GRCh38 chr13: 53,033,949-53,033,949 , GRCh37.p13 chr13: 53,608,084-53,608,084 OLFM4
    nsv5941344copy number variation1nstd209human GRCh38 chr13: 53,051,264-53,051,341 , GRCh37.p13 chr13: 53,625,399-53,625,476 OLFM4
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5553404insertion1nstd206human GRCh38 chr13: 53,033,986-53,034,000 , GRCh37.p13 chr13: 53,608,121-53,608,135 OLFM4
    nsv5498468copy number variation1nstd206human GRCh38 chr13: 53,044,433-53,059,463 , GRCh37.p13 chr13: 53,618,568-53,633,598 OLFM4
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
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