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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4352493copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr11: 54,843,571-58,522,826 , GRCh37.p13 chr11: 55,086,995-58,766,250 , GRCh38.p12 chr11: 55,319,519-58,998,777 CTNND1, SLC43A1, 198 more genes
    nsv4344924mobile element insertion1nstd166human GRCh37.p13 chr11: 3,995,186-73,648,818 , GRCh38.p12 chr11: 3,973,956-73,937,773 ARHGAP1, PHOX2A, 1677 more genes
    nsv4343942sequence alteration1nstd166human GRCh37.p13 chr11: 31,496,919-82,225,032 , GRCh38.p12 chr11: 31,475,372-82,513,990 ACTN3, ALDH3B1, 1280 more genes
    nsv4342806mobile element insertion1nstd166human GRCh37.p13 chr11: 47,392,912-94,663,143 , GRCh38.p12 chr11: 47,371,361-94,929,978 ACTN3, GRK2, 1253 more genes
    nsv4340025sequence alteration1nstd166human GRCh37.p13 chr11: 31,496,808-82,225,043 , GRCh38.p12 chr11: 31,475,261-82,514,001 APLNR, MRPL49, 1280 more genes
    nsv4334790sequence alteration1nstd166human GRCh37.p13 chr11: 33,095,308-83,983,015 , GRCh38.p12 chr11: 33,073,762-84,271,972 ACTN3, ALDH3B1, 1282 more genes
    nsv4314331mobile element insertion1nstd166human GRCh37.p13 chr11: 35,753,682-102,618,200 , GRCh38.p12 chr11: 35,732,134-102,747,469 ALDH3B2, ARHGAP1, 1476 more genes
    nsv4310275insertion1nstd166human GRCh37.p13 chr11: 18,581,666-80,047,938 , GRCh38.p12 chr11: 18,560,119-80,336,894 ARHGAP1, PHOX2A, 1405 more genes
    nsv4307236insertion1nstd166human GRCh37.p13 chr11: 36,529,122-101,428,932 , GRCh38.p12 chr11: 36,507,572-101,558,201 ACTN3, ALDH3B1, 1446 more genes
    nsv4305216insertion1nstd166human GRCh37.p13 chr11: 29,715,873-82,728,921 , GRCh38.p12 chr11: 29,694,326-83,017,879 ALDH3B1, PHOX2A, 1308 more genes
    nsv4302237insertion1nstd166human GRCh37.p13 chr11: 36,277,076-104,293,675 , GRCh38.p12 chr11: 36,255,526-104,422,947 ACTN3, GRK2, 1497 more genes
    nsv4299560insertion1nstd166human GRCh37.p13 chr11: 13,092,185-72,141,529 , GRCh38.p12 chr11: 13,070,638-72,430,485 ACTN3, ALDH3B1, 1330 more genes
    nsv4296187insertion1nstd166human GRCh37.p13 chr11: 37,370,427-89,219,806 , GRCh38.p12 chr11: 37,348,877-89,486,638 ACTN3, GRK2, 1282 more genes
    nsv4292784insertion1nstd166human GRCh37.p13 chr11: 45,565,505-67,868,394 , GRCh38.p12 chr11: 45,543,955-68,100,927 ACP2, GRK2, 826 more genes
    nsv4027394mobile element insertion1nstd166human GRCh37.p13 chr11: 11,671,930-73,892,076 , GRCh38.p12 chr11: 11,650,383-74,181,031 ACP2, GRK2, 1396 more genes
    nsv4024622mobile element insertion1nstd166human GRCh37.p13 chr11: 45,340,441-127,868,875 , GRCh38.p12 chr11: 45,318,890-127,998,980 APLNR, ALDH3B2, 1936 more genes
    nsv4020369mobile element insertion1nstd166human GRCh37.p13 chr11: 20,631,117-106,595,836 , GRCh38.p12 chr11: 20,609,571-106,725,110 BIRC2, MRPL49, 1704 more genes
    nsv4014219mobile element insertion1nstd166human GRCh38.p12 chr11: 41,961,400-90,199,555 , GRCh37.p13 chr11: 41,982,950-89,932,723 MRPL49, CD6, 1287 more genes
    nsv4013213mobile element insertion1nstd166human GRCh37.p13 chr11: 32,080,227-79,009,612 , GRCh38.p12 chr11: 32,058,681-79,298,567 ACP2, GRK2, 1251 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 , NCBI36 (hg18) chr11: 220,616-134,443,680 LOC171391, CTTN, 2899 more genes
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