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 139

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5847138copy number variation1nstd209human GRCh38 chr7: 63,906,432-63,908,431 , GRCh37.p13 chr7: 63,366,810-63,368,809 NMD3P1, LINC02848
    nsv5686339mobile element insertion1nstd211human GRCh38 chr7: 63,912,056-63,912,056 , GRCh37.p13 chr7: 63,372,434-63,372,434 LINC02848
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4957424copy number variation1nstd200human GRCh38 chr7: 63,915,540-63,920,711 , GRCh37.p13 chr7: 63,375,918-63,381,089 LINC02848
    nsv4819290copy number variation1nstd200human GRCh37 chr7: 63,375,918-63,381,089 , GRCh38.p12 chr7: 63,915,540-63,920,711 LINC02848
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4729639copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,508,852-64,940,346 , GRCh38.p12 chr7: 63,048,474-65,475,433 VN1R39P, LOC105375324, 113 more genes
    nsv4728981copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,495,083-64,927,758 , GRCh38.p12 chr7: 63,034,705-65,462,845 LOC105375321, GUSBP6, 113 more genes
    nsv4606786copy number variation1nstd183human GRCh37 chr7: 62,520,372-64,227,496 , GRCh38.p12 chr7: 63,059,994-64,767,118 , LOC105375326, 89 more genes
    nsv4598888copy number variation2nstd183human GRCh37 chr7: 63,370,292-63,847,365 , GRCh38.p12 chr7: 63,909,914-64,386,987 LOC105375322, MTND3P2, 35 more genes
    nsv4524971copy number variation1nstd166human GRCh37.p13 chr7: 63,129,699-63,463,500 , GRCh38.p12 chr7: 63,669,321-64,003,122 , LINC02848, 18 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4144177copy number variation1nstd166human GRCh37.p13 chr7: 63,364,985-63,365,051 , GRCh38.p12 chr7: 63,904,607-63,904,673 LINC02848
    nsv4140164copy number variation1nstd166human GRCh37.p13 chr7: 63,352,508-63,858,518 , GRCh38.p12 chr7: 63,892,130-64,398,140 MTND3P2, VN1R37P, 36 more genes
    nsv4132870copy number variation1nstd166human GRCh37.p13 chr7: 62,491,653-64,942,895 , GRCh38.p12 chr7: 63,031,275-65,477,982 , GUSBP6, 117 more genes
    nsv3962778copy number variation1nstd168human GRCh38 chr7: 63,827,451-64,011,735 , GRCh37.p13 chr7: 63,287,829-63,472,113 , SLC25A1P3, 10 more genes
    nsv3923928copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 62,074,825-65,951,097 , GRCh37 chr7: 62,437,390-66,313,662 , GRCh38 chr7: 62,977,012-66,848,675 ASL, ERV3-1, 153 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 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