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 205

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7065303inversion1nstd229human GRCh38 chr9: 71,473,712-72,923,816 , GRCh37.p13 chr9: 74,088,628-75,538,732 LOC101927234, GDA, 21 more genes
    nsv6873018copy number variation1nstd229human GRCh38 chr9: 72,339,177-72,342,090 , GRCh37.p13 chr9: 74,954,093-74,957,006 LINC01504
    nsv6870276copy number variation1nstd229human GRCh38 chr9: 72,332,701-72,337,000 , GRCh37.p13 chr9: 74,947,617-74,951,916 LINC01504
    nsv6867720copy number variation1nstd229human GRCh38 chr9: 72,302,952-72,314,290 , GRCh37.p13 chr9: 74,917,868-74,929,206 LINC01504
    nsv6865635copy number variation1nstd229human GRCh38 chr9: 72,322,801-72,327,099 , GRCh37.p13 chr9: 74,937,717-74,942,015 LINC01504
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 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
    nsv6570850inversion1nstd223human GRCh38 chr9: 72,327,377-72,328,136 , GRCh37.p13 chr9: 74,942,293-74,943,052 LINC01504
    nsv6570096inversion1nstd223human GRCh38 chr9: 72,327,739-72,327,840 , GRCh37.p13 chr9: 74,942,655-74,942,756 LINC01504
    nsv6448390copy number variation1nstd223human GRCh38 chr9: 72,302,958-72,314,280 , GRCh37.p13 chr9: 74,917,874-74,929,196 LINC01504
    nsv6448261copy number variation1nstd223human GRCh38 chr9: 72,322,801-72,327,094 , GRCh37.p13 chr9: 74,937,717-74,942,010 LINC01504
    nsv6443781copy number variation1nstd223human GRCh38 chr9: 72,307,779-72,311,849 , GRCh37.p13 chr9: 74,922,695-74,926,765 LINC01504
    nsv6435827copy number variation1nstd223human GRCh38 chr9: 72,326,322-72,327,510 , GRCh37.p13 chr9: 74,941,238-74,942,426 LINC01504
    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
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6257725mobile element insertion1nstd215human GRCh38 chr9: 72,320,318-72,320,318 , GRCh37.p13 chr9: 74,935,234-74,935,234 LINC01504
    nsv6137094copy number variation1nstd213human GRCh37 chr9: 71,840,000-78,800,001 , GRCh38.p12 chr9: 69,225,084-76,185,085 KLF9, PCSK5, 83 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