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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
    nsv4676037copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,734,337-126,944,508 , GRCh38.p12 chr11: 126,864,442-127,074,613 LOC105369558, KIRREL3-AS2, 5 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4673961copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583 OR8A2P, LOC101929473, 186 more genes
    nsv4456524copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,111,090-127,755,537 , GRCh38.p12 chr11: 126,241,195-127,885,642 LOC107984379, RPL35AP26, 23 more genes
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 LINC02098, LOC105369587, 276 more genes
    nsv4350042copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,446,101-134,904,063 , GRCh38.p12 chr11: 125,576,205-135,034,169 SNX19, TP53AIP1, 138 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4349032copy number variation1nstd102humanPathogenic GRCh37 chr11: 126,809,705-130,289,168 , GRCh38.p12 chr11: 126,939,809-130,419,273 LINC01395, LOC399975, 53 more genes
    nsv3924932copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,761,210-128,942,286 , GRCh38 chr11: 125,891,315-129,072,391 , NCBI36 chr11: 125,266,420-128,447,496 KCNJ1, LOC107984409, 52 more genes
    nsv3924566copy number variation1nstd102humanPathogenic GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160 CCDC15-DT, LOC105369544, 271 more genes
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
    nsv3923251copy number variation1nstd102humanPathogenic NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165 KIRREL3-AS3, OR8B4, 279 more genes
    nsv3922795copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,564,750-127,839,010 , GRCh38 chr11: 126,694,855-127,969,115 , NCBI36 chr11: 126,069,960-127,344,220 LOC101929473, RN7SKP121, 13 more genes
    nsv3922773copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617 ETS1-AS1, SLC37A2, 301 more genes
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