U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 162

    loading data ...

    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
    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
    nsv6996450copy number variation1nstd229human GRCh38 chr17: 43,897,609-43,948,664 , GRCh37.p13 chr17: 41,974,977-42,026,032 PPY, FAM215A, 6 more genes
    nsv6989081copy number variation1nstd229human GRCh38 chr17: 43,943,768-43,943,980 , GRCh37.p13 chr17: 42,021,136-42,021,348 PPY
    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
    nsv6978218copy number variation1nstd229human GRCh38 chr17: 43,884,752-44,008,192 , GRCh37.p13 chr17: 41,962,120-42,085,560 PPY, LOC102724183, 8 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
    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
    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
    nsv5013731copy number variation1nstd200human GRCh38 chr17: 43,853,861-43,976,344 , GRCh37.p13 chr17: 41,931,229-42,053,712 , LINC01976, 10 more genes
    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
    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
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center