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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146479copy number variation1nstd232human GRCh37.p13 chr11: 65,738,992-65,739,052 , GRCh38.p12 chr11: 65,971,521-65,971,581 SART1
    nsv7143140copy number variation1nstd232human GRCh37.p13 chr11: 65,735,056-65,735,147 , GRCh38.p12 chr11: 65,967,585-65,967,676 SART1
    nsv7139098copy number variation1nstd232human GRCh37.p13 chr11: 65,734,851-65,734,937 , GRCh38.p12 chr11: 65,967,380-65,967,466 SART1
    nsv7137467copy number variation1nstd232human GRCh37.p13 chr11: 65,733,455-65,733,543 , GRCh38.p12 chr11: 65,965,984-65,966,072 SART1
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7066157inversion1nstd229human GRCh38 chr11: 65,959,822-65,959,927 , GRCh37.p13 chr11: 65,727,293-65,727,398 SART1, TSGA10IP
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6914921copy number variation1nstd229human GRCh38 chr11: 65,667,113-66,107,104 , GRCh37.p13 chr11: 65,434,584-65,874,575 SNX32, OVOL1, 28 more genes
    nsv6914636copy number variation1nstd229human GRCh38 chr11: 65,968,383-65,972,265 , GRCh37.p13 chr11: 65,735,854-65,739,736 SART1
    nsv6913523copy number variation1nstd229human GRCh38 chr11: 65,973,651-65,986,956 , GRCh37.p13 chr11: 65,741,122-65,754,427 LOC100420020, SART1
    nsv6909952copy number variation1nstd229human GRCh38 chr11: 65,959,931-65,960,291 , GRCh37.p13 chr11: 65,727,402-65,727,762 SART1, TSGA10IP
    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
    nsv6468636copy number variation1nstd223human GRCh38 chr11: 65,973,651-65,986,956 , GRCh37.p13 chr11: 65,741,122-65,754,427 SART1, LOC100420020
    nsv6457887copy number variation1nstd223human GRCh38 chr11: 65,960,669-65,967,340 , GRCh37.p13 chr11: 65,728,140-65,734,811 TSGA10IP, SART1
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 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
    nsv6303074copy number variation1nstd186human GRCh37 chr11: 65,723,594-65,728,101 , GRCh38.p12 chr11: 65,956,123-65,960,630 SART1, TSGA10IP
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