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 190

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7098895copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471 LOC105371512, EIF4A1, 61 more genes
    nsv7095414copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936 CTC1, SAT2, 103 more genes
    nsv7095413copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,123,304-7,606,804 , GRCh38.p12 chr17: 7,219,985-7,703,486 MPDU1, PLSCR3, 50 more genes
    nsv7095410copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,606,804 , GRCh38.p12 chr17: 6,425,460-7,703,486 PITPNM3, SLC2A4, 85 more genes
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 MIR324, SLC2A4, 101 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6995956copy number variation1nstd229human GRCh38 chr17: 7,211,801-7,562,200 , GRCh37.p13 chr17: 7,115,120-7,465,517 DVL2, SPEM2, 34 more genes
    nsv6995921copy number variation1nstd229human GRCh38 chr17: 7,433,470-7,438,075 , GRCh37.p13 chr17: 7,336,789-7,341,394 FGF11, TMEM102
    nsv6992449copy number variation1nstd229human GRCh38 chr17: 7,427,331-7,481,950 , GRCh37.p13 chr17: 7,330,650-7,385,269 TMEM102, ZBTB4, 5 more genes
    nsv6988561copy number variation1nstd229human GRCh38 chr17: 7,433,015-7,439,073 , GRCh37.p13 chr17: 7,336,334-7,342,392 FGF11, TMEM102, 1 more genes
    nsv6986139copy number variation1nstd229human GRCh38 chr17: 7,433,101-7,434,400 , GRCh37.p13 chr17: 7,336,420-7,337,719 TMEM102, SPEM3
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6591119inversion1nstd223human GRCh38 chr17: 5,860,086-7,699,509 , GRCh37.p13 chr17: 5,763,406-7,602,827 RPL23AP73, MIR195, 90 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6507483copy number variation1nstd223human GRCh38 chr17: 7,433,140-7,434,359 , GRCh37.p13 chr17: 7,336,459-7,337,678 SPEM3, TMEM102
    nsv6314103copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972 RPL7AP64, TNK1, 87 more genes
    nsv6133424copy number variation2nstd213human GRCh37 chr17: 7,240,000-7,460,001 , GRCh38.p12 chr17: 7,336,681-7,556,684 , GRCh38.p12 chr17|NW_016107299.1: 1-154,723 CHRNB1, FGF11, 18 more genes
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 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