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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098935copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,603,558-44,033,313 , GRCh37.p13 chr17: 41,680,926-42,110,681 LOC107985086, MPP2, 21 more genes
    nsv7059460inversion1nstd229human GRCh38 chr17: 44,003,191-44,012,094 , GRCh37.p13 chr17: 42,080,559-42,089,462 TMEM101, NAGS, 1 more genes
    nsv6996751copy number variation1nstd229human GRCh38 chr17: 43,867,655-44,022,455 , GRCh37.p13 chr17: 41,945,023-42,099,823 PYY, LINC01976, 9 more genes
    nsv6988154copy number variation1nstd229human GRCh38 chr17: 44,021,901-44,024,900 , GRCh37.p13 chr17: 42,099,269-42,102,268 TMEM101
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6624081copy number variation1nstd224human GRCh37 chr17: 41,946,180-42,091,769 , GRCh38.p12 chr17: 43,868,812-44,014,401 PPY, TMEM101, 9 more genes
    nsv6513091copy number variation1nstd223human GRCh38 chr17: 44,017,106-44,017,549 , GRCh37.p13 chr17: 42,094,474-42,094,917 TMEM101
    nsv6507361copy number variation1nstd223human GRCh38 chr17: 43,844,289-44,031,089 , GRCh37.p13 chr17: 41,921,657-42,108,457 PYY, LOC107985077, 12 more genes
    nsv6500684copy number variation1nstd223human GRCh38 chr17: 44,019,301-44,023,200 , GRCh37.p13 chr17: 42,096,669-42,100,568 TMEM101
    nsv6291646copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,085,508-42,361,563 , GRCh38.p12 chr17: 44,008,140-44,284,195 LOC105371790, HDAC5, 16 more genes
    nsv6133311copy number variation3nstd213human GRCh37 chr17: 41,970,000-42,760,001 , GRCh38.p12 chr17: 43,892,632-44,682,633 FZD2, GRN, 43 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5016495copy number variation1nstd200human GRCh38 chr17: 44,019,179-44,023,099 , GRCh37.p13 chr17: 42,096,547-42,100,467 TMEM101
    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
    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
    nsv4576088mobile element insertion1nstd166human GRCh37.p13 chr17: 42,087,824-42,087,824 , GRCh38.p12 chr17: 44,010,456-44,010,456 TMEM101
    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
    nsv3921189copy number variation1nstd102humanUncertain significance NCBI36 chr17: 39,298,066-39,477,792 , GRCh37.p13 chr17: 41,942,540-42,122,266 , GRCh38.p12 chr17: 43,865,172-44,044,898 LSM12, PYY, 10 more genes
    nsv3919609copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,648,246-42,839,745 , GRCh38 chr17: 43,570,878-44,762,377 , NCBI36 chr17: 39,003,772-40,195,271 SMCO4P1, LINC01180, 59 more genes
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