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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6993017copy number variation1nstd229human GRCh38 chr17: 50,426,702-50,566,153 , GRCh37.p13 chr17: 48,504,063-48,643,514 CHAD, RSAD1, 8 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6624253copy number variation1nstd224human GRCh37 chr17: 48,509,965-48,631,681 , GRCh38.p12 chr17: 50,432,604-50,554,320 CHAD, EPN3, 7 more genes
    nsv6516290copy number variation1nstd223human GRCh38 chr17: 50,521,281-50,530,853 , GRCh37.p13 chr17: 48,598,642-48,608,214 MYCBPAP, EPN3
    nsv6202727copy number variation1nstd214human GRCh38 chr17: 50,534,063-50,534,140 , GRCh37.p13 chr17: 48,611,424-48,611,501 EPN3
    nsv6133067copy number variation1nstd213human GRCh37 chr17: 48,530,000-48,770,001 , GRCh38.p12 chr17: 50,452,639-50,692,640 CHAD, EPN3, 10 more genes
    nsv6026179copy number variation1nstd212human GRCh38 chr17: 50,426,696-50,566,152 , GRCh37.p13 chr17: 48,504,057-48,643,513 CACNA1G-AS1, MRPS21P9, 8 more genes
    nsv6021906copy number variation1nstd212human GRCh38 chr17: 50,534,079-50,534,156 , GRCh37.p13 chr17: 48,611,440-48,611,517 EPN3
    nsv5944756copy number variation1nstd209human GRCh38 chr17: 50,534,063-50,534,140 , GRCh37.p13 chr17: 48,611,424-48,611,501 EPN3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5326096copy number variation1nstd204human GRCh37.p13 chr17: 48,598,883-48,608,235 , GRCh38.p13 chr17: 50,521,522-50,530,874 EPN3, 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
    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
    nsv4264644copy number variation1nstd166human GRCh37.p13 chr17: 48,598,908-48,608,213 , GRCh38.p12 chr17: 50,521,547-50,530,852 EPN3, 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
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