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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
    nsv5972651insertion1nstd209human GRCh38 chr17: 50,522,709-50,522,709 , GRCh37.p13 chr17: 48,600,070-48,600,070 MYCBPAP
    nsv5933048copy number variation1nstd209human GRCh38 chr17: 50,530,463-50,530,515 , GRCh37.p13 chr17: 48,607,824-48,607,876 MYCBPAP
    nsv5655376insertion1nstd207human GRCh38 chr17: 50,519,762-50,519,762 , GRCh37.p13 chr17: 48,597,123-48,597,123 MYCBPAP
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5523282copy number variation1nstd206human GRCh38 chr17: 50,530,463-50,530,516 , GRCh37.p13 chr17: 48,607,824-48,607,877 MYCBPAP
    nsv5521771copy number variation1nstd206human GRCh38 chr17: 50,512,838-50,512,946 , GRCh37.p13 chr17: 48,590,199-48,590,307 MYCBPAP
    nsv5326096copy number variation1nstd204human GRCh37.p13 chr17: 48,598,883-48,608,235 , GRCh38.p13 chr17: 50,521,522-50,530,874 EPN3, MYCBPAP
    nsv5299905copy number variation1nstd204human GRCh38.p13 chr17: 50,527,924-50,529,223 , GRCh37.p13 chr17: 48,605,285-48,606,584 MYCBPAP
    nsv5289682copy number variation1nstd204human GRCh38.p13 chr17: 50,520,873-50,530,886 , GRCh37.p13 chr17: 48,598,234-48,608,247 MYCBPAP, EPN3
    nsv5284227copy number variation1nstd204human GRCh38.p13 chr17: 50,521,601-50,530,900 , GRCh37.p13 chr17: 48,598,962-48,608,261 EPN3, MYCBPAP
    nsv5026386copy number variation1nstd200human GRCh38 chr17: 50,521,547-50,530,852 , GRCh37.p13 chr17: 48,598,908-48,608,213 MYCBPAP, EPN3
    nsv5013808copy number variation1nstd200human GRCh38 chr17: 50,448,125-50,521,134 , GRCh37.p13 chr17: 48,525,486-48,598,495 MRPS21P9, CHAD, 3 more genes
    nsv4867259copy number variation1nstd200human GRCh37 chr17: 48,598,908-48,608,213 , GRCh38.p12 chr17: 50,521,547-50,530,852 EPN3, MYCBPAP
    nsv4629138copy number variation1nstd183human GRCh37 chr17: 48,579,452-48,630,246 , GRCh38.p12 chr17: 50,502,091-50,552,885 LOC105371824, SPATA20, 2 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
    nsv4266313copy number variation1nstd166human GRCh37.p13 chr17: 48,525,486-48,598,506 , GRCh38.p12 chr17: 50,448,125-50,521,145 ACSF2, CHAD, 3 more genes
    nsv4264644copy number variation1nstd166human GRCh37.p13 chr17: 48,598,908-48,608,213 , GRCh38.p12 chr17: 50,521,547-50,530,852 EPN3, MYCBPAP
    nsv4254821copy number variation1nstd166human GRCh37.p13 chr17: 48,607,824-48,607,877 , GRCh38.p12 chr17: 50,530,463-50,530,516 MYCBPAP
    nsv4254749copy number variation1nstd166human GRCh37.p13 chr17: 48,503,985-48,643,548 , GRCh38.p12 chr17: 50,426,624-50,566,187 RSAD1, MRPS21P9, 8 more genes
    nsv3969055copy number variation1nstd168human GRCh38 chr17: 50,480,565-50,509,003 , GRCh37.p13 chr17: 48,557,926-48,586,364 RSAD1, MYCBPAP
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