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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4630253copy number variation1nstd183human GRCh37 chr17: 80,043,487-80,045,226 , GRCh38.p12 chr17: 82,085,611-82,087,350 FASN
    nsv4629871copy number variation1nstd183human GRCh37 chr17: 80,046,240-80,046,382 , GRCh38.p12 chr17: 82,088,364-82,088,506 SNORD134, FASN
    nsv4629184copy number variation1nstd183human GRCh37 chr17: 79,981,915-80,146,485 , GRCh38.p12 chr17: 82,024,039-82,188,609 RAC3, DCXR-DT, 8 more genes
    nsv4629052copy number variation1nstd183human GRCh37 chr17: 80,056,102-80,056,152 , GRCh38.p12 chr17: 82,098,226-82,098,276 FASN
    nsv4619638copy number variation1nstd183human GRCh37 chr17: 79,785,999-81,060,000 , GRCh38.p12 chr17: 81,828,123-83,101,964 , PCYT2, 55 more genes
    nsv4618971copy number variation1nstd183human GRCh37 chr17: 80,044,501-80,053,300 , GRCh38.p12 chr17: 82,086,625-82,095,424 SNORD134, FASN
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457495copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,663,313-80,197,463 , GRCh38.p12 chr17: 81,696,283-82,239,587 NOTUM, PPP1R27, 34 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4438075copy number variation1nstd175human GRCh37 chr17: 80,039,760-80,039,818 , GRCh38.p12 chr17: 82,081,884-82,081,942 FASN
    nsv4414464copy number variation1nstd174human GRCh37 chr17: 80,031,828-80,139,700 , GRCh38.p12 chr17: 82,073,952-82,181,824 CCDC57, SNORD134, 1 more genes
    nsv4414408copy number variation1nstd174human GRCh37 chr17: 80,039,039-80,053,492 , GRCh38.p12 chr17: 82,081,163-82,095,616 SNORD134, FASN
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv4269043copy number variation1nstd166human GRCh37.p13 chr17: 79,906,988-80,794,330 , GRCh38.p12 chr17: 81,949,112-82,836,454 , NOTUM, 39 more genes
    nsv3958956insertion1nstd168human GRCh38 chr17: 82,064,467-82,078,906 , GRCh37.p13 chr17: 80,022,343-80,036,782 FASN, DUS1L
    nsv3934458copy number variation1nstd167human GRCh37 chr17: 80,039,760-80,039,818 , GRCh38.p12 chr17: 82,081,884-82,081,942 FASN
    nsv3922435copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 77,623,503-78,653,717 , GRCh37 chr17: 80,030,214-81,048,189 , GRCh38 chr17: 82,072,338-83,102,552 CD7, CSNK1D, 28 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 more genes
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