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 658

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070730inversion1nstd229human GRCh38 chr9: 62,058,130-67,204,238 , GRCh37.p13 chr9: 41,204,320-44,676,072 ATP5F1AP10, IGKV1OR9-1, 125 more genes
    nsv7065088inversion1nstd229human GRCh38 chr9: 66,910,436-67,624,629 , GRCh37.p13 chr9: 65,637,442-67,692,075 LOC105379450, CNTNAP3P2, 11 more genes
    nsv7064084inversion1nstd229human GRCh38 chr9: 64,120,773-68,530,496 , GRCh37.p13 chr9: 40,041,911-44,672,613 LOC112267859, ZNG1C, 91 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633912copy number variation7nstd224human GRCh37 chr9: 40,614,575-40,813,425 , GRCh38.p12 chr9: 66,879,416-67,078,266 ZNF658, LOC642490, 4 more genes
    nsv6633911copy number variation1nstd224human GRCh37 chr9: 40,614,575-40,813,310 , GRCh38.p12 chr9: 66,879,531-67,078,266 ZNF658, LOC642490, 4 more genes
    nsv6633525copy number variation1nstd224human GRCh37 chr9: 40,614,575-40,799,158 , GRCh38.p12 chr9: 66,893,683-67,078,266 SPATA31A3, FAM74A3, 3 more genes
    nsv6633524copy number variation1nstd224human GRCh37 chr9: 40,484,265-40,813,425 , GRCh38.p12 chr9: 66,879,416-67,208,576 ZNF658, LOC642490, 7 more genes
    nsv6633456copy number variation1nstd224human GRCh37 chr9: 40,484,265-40,774,588 , GRCh38.p12 chr9: 66,918,253-67,208,576 ZNF658, CNTNAP3P2, 6 more genes
    nsv6453495copy number variation1nstd223human GRCh38 chr9: 67,093,601-67,094,500 , GRCh37.p13 chr9: 40,598,341-40,599,240 CNTNAP3P2
    nsv6449175copy number variation1nstd223human GRCh38 chr9: 67,067,801-67,072,600 , GRCh37.p13 chr9: 40,620,241-40,625,040 CNTNAP3P2
    nsv6444855copy number variation1nstd223human GRCh38 chr9: 67,055,001-67,059,500 , GRCh37.p13 chr9: 40,633,341-40,637,840 CNTNAP3P2
    nsv6440774copy number variation1nstd223human GRCh38 chr9: 67,087,001-67,095,600 , GRCh37.p13 chr9: 40,597,241-40,605,840 CNTNAP3P2, USP12P3
    nsv6440284copy number variation1nstd223human GRCh38 chr9: 67,089,201-67,092,300 , GRCh37.p13 chr9: 40,600,541-40,603,640 CNTNAP3P2
    nsv6438174copy number variation1nstd223human GRCh38 chr9: 67,065,001-67,066,700 , GRCh37.p13 chr9: 40,626,141-40,627,840 CNTNAP3P2
    nsv6315415copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-68,342,786 , GRCh38.p12 chr9: 203,861-67,920,552 LOC107987068, FAM74A7, 846 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314461complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr9: 67,065,150-67,065,150 , GRCh38.p12 chr9: 67,065,152-67,065,152 , GRCh37 chr9: 40,627,689-40,627,689 , GRCh37 chr9: 40,627,691-40,627,691 , GRCh38.p12 chr8: 43,213,594-43,213,594 , GRCh38.p12 chr8: 43,213,595-43,213,595 , GRCh37 chr8: 43,068,737-43,068,737 , GRCh37 chr8: 43,068,738-43,068,738 CNTNAP3P2
    nsv6313827copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-84,155,399 , GRCh38.p12 chr9: 203,861-81,540,484 RPSAP75, ANKRD20A2P, 1008 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 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