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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138532copy number variation1nstd232human GRCh37.p13 chr11: 64,785,945-64,786,040 , GRCh38.p12 chr11: 65,018,473-65,018,568 ARL2, ARL2-SNX15, 1 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv6915986copy number variation1nstd229human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 TM7SF2, HIGD1AP10, 19 more genes
    nsv6913417copy number variation1nstd229human GRCh38 chr11: 65,009,206-65,018,775 , GRCh37.p13 chr11: 64,776,678-64,786,247 ARL2-SNX15, ARL2, 1 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6470631copy number variation1nstd223human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 MAJIN, HIGD1AP10, 19 more genes
    nsv6466732copy number variation1nstd223human GRCh38 chr11: 65,019,249-65,022,926 , GRCh37.p13 chr11: 64,786,721-64,790,398 ARL2-SNX15, ARL2
    nsv6466122copy number variation1nstd223human GRCh38 chr11: 65,006,087-65,024,224 , GRCh37.p13 chr11: 64,773,559-64,791,696 ARL2-SNX15, ARL2, 2 more genes
    nsv6465748copy number variation1nstd223human GRCh38 chr11: 65,019,377-65,024,169 , GRCh37.p13 chr11: 64,786,849-64,791,641 EEF1A1P18, ARL2-SNX15, 1 more genes
    nsv6459548copy number variation1nstd223human GRCh38 chr11: 65,013,083-65,013,777 , GRCh37.p13 chr11: 64,780,555-64,781,249 ARL2-SNX15, ARL2
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5509183copy number variation1nstd206human GRCh38 chr11: 65,009,186-65,018,797 , GRCh37.p13 chr11: 64,776,658-64,786,269 ARL2-SNX15, MIR6879, 1 more genes
    nsv5505759copy number variation1nstd206human GRCh38 chr11: 65,011,136-65,018,701 , GRCh37.p13 chr11: 64,778,608-64,786,173 ARL2, ARL2-SNX15, 1 more genes
    nsv5501942copy number variation1nstd206human GRCh38 chr11: 65,021,016-65,021,092 , GRCh37.p13 chr11: 64,788,488-64,788,564 ARL2-SNX15, ARL2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5309939copy number variation1nstd204human GRCh38.p13 chr11: 65,005,642-65,024,522 , GRCh37.p13 chr11: 64,773,114-64,791,994 MIR6879, ARL2, 2 more genes
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