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Items: 1 to 20 of 936

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141292copy number variation1nstd232human GRCh37.p13 chr1: 963,864-963,924 , GRCh38.p12 chr1: 1,028,484-1,028,544 AGRN
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7096012copy number variation1nstd102humanUncertain significance GRCh37 chr1: 980,719-1,168,648 , GRCh38.p12 chr1: 1,045,339-1,233,268 SDF4, TNFRSF18, 13 more genes
    nsv7096011copy number variation1nstd102humanUncertain significance GRCh37 chr1: 955,553-957,862 , GRCh38.p12 chr1: 1,020,173-1,022,482 AGRN
    nsv7093565insertion1nstd102humanUncertain significance GRCh38 chr1: 1,049,050-1,049,050 , GRCh37 chr1: 984,430-984,430 AGRN
    nsv7054612inversion1nstd229human GRCh38 chr1: 972,727-1,033,183 , GRCh37.p13 chr1: 908,107-968,563 PLEKHN1, PERM1, 4 more genes
    nsv7050001inversion1nstd229human GRCh38 chr1: 987,061-1,079,323 , GRCh37.p13 chr1: 922,441-1,014,703 LOC100288175, RNF223, 5 more genes
    nsv7048107inversion1nstd229human GRCh38 chr1: 1,025,877-1,028,193 , GRCh37.p13 chr1: 961,257-963,573 AGRN
    nsv7046830inversion1nstd229human GRCh38 chr1: 1,031,989-1,075,884 , GRCh37.p13 chr1: 967,369-1,011,264 LOC100288175, RNF223, 2 more genes
    nsv7045793inversion1nstd229human GRCh38 chr1: 1,031,265-1,036,698 , GRCh37.p13 chr1: 966,645-972,078 AGRN
    nsv7040598inversion1nstd229human GRCh38 chr1: 1,016,054-1,174,806 , GRCh37.p13 chr1: 951,434-1,110,186 MIR200A, LINC01342, 9 more genes
    nsv6658041copy number variation1nstd229human GRCh38 chr1: 989,189-1,068,550 , GRCh37.p13 chr1: 924,569-1,003,930 HES4, AGRN, 4 more genes
    nsv6658013copy number variation1nstd229human GRCh38 chr1: 980,590-1,074,345 , GRCh37.p13 chr1: 915,970-1,009,725 LOC105378948, RNF223, 6 more genes
    nsv6657952copy number variation1nstd229human GRCh38 chr1: 987,901-1,026,800 , GRCh37.p13 chr1: 923,281-962,180 ISG15, HES4, 2 more genes
    nsv6657906copy number variation1nstd229human GRCh38 chr1: 998,176-1,020,513 , GRCh37.p13 chr1: 933,556-955,893 HES4, AGRN, 2 more genes
    nsv6657199copy number variation1nstd229human GRCh38 chr1: 926,615-1,239,899 , GRCh37.p13 chr1: 861,995-1,175,279 TTLL10-AS1, MIR200B, 21 more genes
    nsv6656705copy number variation1nstd229human GRCh38 chr1: 872,040-1,151,798 , GRCh37.p13 chr1: 807,420-1,087,178 C1orf159, LOC105378948, 17 more genes
    nsv6656142copy number variation1nstd229human GRCh38 chr1: 838,653-1,166,615 , GRCh37.p13 chr1: 774,033-1,101,995 LINC01128, SAMD11, 21 more genes
    nsv6655873copy number variation1nstd229human GRCh38 chr1: 829,470-1,107,141 , GRCh37.p13 chr1: 764,850-1,042,521 LOC107985728, PERM1, 18 more genes
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