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Items: 1 to 20 of 177

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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
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 more genes
    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
    nsv6980328copy number variation1nstd229human GRCh38 chr17: 43,854,001-43,871,500 , GRCh37.p13 chr17: 41,931,369-41,948,868 CD300LG, LOC107985077
    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
    nsv6314057copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,202,796-41,974,964 , GRCh38.p12 chr17: 43,050,779-43,897,596 TMEM106A, MPP2, 33 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
    nsv5517445copy number variation1nstd206human GRCh38 chr17: 43,862,438-43,888,393 , GRCh37.p13 chr17: 41,939,806-41,965,761 CD300LG, MPP2
    nsv5325405copy number variation1nstd204human GRCh38.p13 chr17: 43,862,433-43,888,402 , GRCh37.p13 chr17: 41,939,801-41,965,770 CD300LG, MPP2
    nsv5292398copy number variation1nstd204human GRCh38.p13 chr17: 43,862,450-43,888,138 , GRCh37.p13 chr17: 41,939,818-41,965,506 MPP2, CD300LG
    nsv5013732copy number variation1nstd200human GRCh38 chr17: 43,862,438-43,888,393 , GRCh37.p13 chr17: 41,939,806-41,965,761 CD300LG, MPP2
    nsv5013731copy number variation1nstd200human GRCh38 chr17: 43,853,861-43,976,344 , GRCh37.p13 chr17: 41,931,229-42,053,712 , LINC01976, 10 more genes
    nsv4864666copy number variation1nstd200human GRCh37 chr17: 41,939,806-41,965,761 , GRCh38.p12 chr17: 43,862,438-43,888,393 CD300LG, MPP2
    nsv4864665copy number variation1nstd200human GRCh37 chr17: 41,931,229-42,053,712 , GRCh38.p12 chr17: 43,853,861-43,976,344 , FAM215A, 10 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
    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
    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
    nsv3923117copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,080,123-43,897,875 , NCBI36 chr17: 38,485,666-39,330,769 , GRCh37 chr17: 41,232,140-41,975,243 RNU6-470P, CCDC200, 33 more genes
    nsv3922353copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,088,882-43,865,172 , GRCh37 chr17: 41,240,899-41,942,540 , NCBI36 chr17: 38,494,425-39,298,066 NBR1, LOC107985077, 31 more genes
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