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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997671copy number variation1nstd229human GRCh38 chr17: 76,732,086-76,732,231 , GRCh37.p13 chr17: 74,728,168-74,728,313 SRSF2, METTL23
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6534265copy number variation1nstd223human GRCh38 chr17: 76,734,038-76,743,570 , GRCh37.p13 chr17: 74,730,120-74,739,652 MFSD11, SRSF2, 2 more genes
    nsv6530843copy number variation1nstd223human GRCh38 chr17: 76,735,301-77,145,300 , GRCh37.p13 chr17: 74,731,383-75,141,382 SEC14L1, RNU6-97P, 12 more genes
    nsv6524942copy number variation1nstd223human GRCh38 chr17: 76,730,751-76,732,417 , GRCh37.p13 chr17: 74,726,833-74,728,499 SRSF2, METTL23
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6197419copy number variation1nstd214human GRCh38 chr17: 76,732,086-76,732,230 , GRCh37.p13 chr17: 74,728,168-74,728,312 SRSF2, METTL23
    nsv5936803copy number variation1nstd209human GRCh38 chr17: 76,732,086-76,732,230 , GRCh37.p13 chr17: 74,728,168-74,728,312 SRSF2, METTL23
    nsv5563569sequence alteration1nstd206human GRCh37.p13 chr17: 74,682,310-74,791,072 , GRCh38 chr17: 76,686,228-76,794,990 SRSF2, JMJD6, 6 more genes
    nsv5283666copy number variation1nstd204human GRCh37.p13 chr17: 74,676,083-74,731,882 , GRCh38.p13 chr17: 76,680,001-76,735,800 SRSF2, JMJD6, 5 more genes
    nsv5186979mobile element insertion1nstd203human GRCh38 chr17: 76,735,304-76,735,315 , GRCh37.p13 chr17: 74,731,386-74,731,397 SRSF2, MFSD11, 1 more genes
    nsv5016772copy number variation1nstd200human GRCh38 chr17: 76,734,039-76,743,570 , GRCh37.p13 chr17: 74,730,121-74,739,652 SRSF2, MFSD11, 2 more genes
    nsv4859042copy number variation1nstd200human GRCh37 chr17: 74,728,201-74,728,314 , GRCh38.p12 chr17: 76,732,119-76,732,232 SRSF2, METTL23
    nsv4676341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041 CYCSP40, RNU6-97P, 38 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4654925copy number variation2nstd186human GRCh37 chr17: 74,728,202-74,728,313 , GRCh38.p12 chr17: 76,732,120-76,732,231 SRSF2, METTL23
    nsv4632383copy number variation1nstd183human GRCh37 chr17: 74,721,845-74,733,918 , GRCh38.p12 chr17: 76,725,763-76,737,836 MFSD11, METTL23, 3 more genes
    nsv4563813sequence alteration1nstd166human GRCh37.p13 chr17: 74,682,236-74,791,072 , GRCh38.p12 chr17: 76,686,154-76,794,990 SRSF2, JMJD6, 6 more genes
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