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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932567copy number variation1nstd209human GRCh38 chr17: 43,638,994-43,639,768 , GRCh37.p13 chr17: 41,716,362-41,717,136 MEOX1
    nsv5701526mobile element insertion1nstd211human GRCh38 chr17: 43,655,686-43,655,686 , GRCh37.p13 chr17: 41,733,054-41,733,054 MEOX1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5517243copy number variation1nstd206human GRCh38 chr17: 43,648,630-43,650,435 , GRCh37.p13 chr17: 41,725,998-41,727,803 MEOX1
    nsv5514298copy number variation1nstd206human GRCh38 chr17: 43,639,126-43,639,804 , GRCh37.p13 chr17: 41,716,494-41,717,172 MEOX1
    nsv5392965copy number variation1nstd186human GRCh37 chr17: 41,716,308-41,717,172 , GRCh38.p12 chr17: 43,638,940-43,639,804 MEOX1
    nsv5391790copy number variation1nstd186human GRCh37 chr17: 41,716,307-41,717,226 , GRCh38.p12 chr17: 43,638,939-43,639,858 MEOX1
    nsv5158743mobile element insertion1nstd203human GRCh38 chr17: 43,653,721-43,653,744 , GRCh37.p13 chr17: 41,731,089-41,731,112 MEOX1
    nsv5013730copy number variation1nstd200human GRCh38 chr17: 43,638,938-43,639,859 , GRCh37.p13 chr17: 41,716,306-41,717,227 MEOX1
    nsv4864664copy number variation1nstd200human GRCh37 chr17: 41,716,297-41,717,186 , GRCh38.p12 chr17: 43,638,929-43,639,818 MEOX1
    nsv4729870copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,221,565-41,775,043 , GRCh38.p12 chr17: 43,069,548-43,697,675 LOC105371785, RNU6-406P, 24 more genes
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4675549copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-41,736,186 , GRCh38.p12 chr17: 43,322,528-43,658,818 DHX8, RNU6-1137P, 12 more genes
    nsv4674980copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,399,892-42,125,780 , GRCh38.p12 chr17: 43,322,528-44,048,412 RPL29P31, MEOX1, 34 more genes
    nsv4457708copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,440,122-41,745,139 , GRCh38.p12 chr17: 43,362,754-43,667,771 RNU2-4P, RNU6-470P, 13 more genes
    nsv4432535copy number variation1nstd172human GRCh37.p13 chr17: 41,728,476-41,728,963 , GRCh38.p12 chr17: 43,651,108-43,651,595 MEOX1
    nsv4421838copy number variation1nstd174human GRCh37 chr17: 41,399,657-41,869,317 , GRCh38.p12 chr17: 43,322,294-43,791,949 LINC00910, LINC02594, 18 more genes
    nsv4368311copy number variation1nstd173human GRCh37 chr17: 41,384,516-42,395,351 , GRCh38.p12 chr17: 43,307,154-44,317,983 , LOC105371789, 55 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4270694copy number variation1nstd166human GRCh37.p13 chr17: 41,722,538-41,722,620 , GRCh38.p12 chr17: 43,645,170-43,645,252 MEOX1
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