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 413

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5254786copy number variation1nstd204human GRCh38.p13 chr7: 143,752,901-143,764,600 , GRCh37.p13 chr7: 143,449,994-143,461,693 CTAGE6, RNU6-267P
    nsv5253972copy number variation1nstd204human GRCh38.p13 chr7: 143,745,001-143,801,800 , GRCh37.p13 chr7: 143,442,094-143,498,893 CTAGE6, RNU6-267P, 2 more genes
    nsv5253205copy number variation1nstd204human GRCh38.p13 chr7: 143,749,101-143,755,900 , GRCh37.p13 chr7: 143,446,194-143,452,993 CTAGE6, RNU6-267P
    nsv5251884copy number variation1nstd204human GRCh38.p13 chr7: 143,744,601-143,761,700 , GRCh37.p13 chr7: 143,441,694-143,458,793 CTAGE6, RNU6-267P
    nsv5251078copy number variation1nstd204human GRCh38.p13 chr7: 143,744,401-143,774,200 , GRCh37.p13 chr7: 143,441,494-143,471,293 CTAGE6, RNU6-267P
    nsv5249813copy number variation1nstd204human GRCh38.p13 chr7: 143,752,901-143,762,000 , GRCh37.p13 chr7: 143,449,994-143,459,093 RNU6-267P, CTAGE6
    nsv5249374copy number variation1nstd204human GRCh38.p13 chr7: 143,744,501-143,801,800 , GRCh37.p13 chr7: 143,441,594-143,498,893 RNU6-267P, RPL26P24, 2 more genes
    nsv5242071copy number variation1nstd204human GRCh38.p13 chr7: 143,750,901-143,767,400 , GRCh37.p13 chr7: 143,447,994-143,464,493 RNU6-267P, CTAGE6
    nsv5240598copy number variation1nstd204human GRCh38.p13 chr7: 143,756,201-143,757,900 , GRCh37.p13 chr7: 143,453,294-143,454,993 CTAGE6
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4730194inversion12nstd198human GRCh37.p13 chr7: 143,284,235-143,546,161 , GRCh38 chr7: 143,587,142-143,849,068 LOC154761, TCAF2, 9 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4679160copy number variation1nstd189human GRCh37.p13 chr7: 143,421,819-143,974,156 , GRCh38.p12 chr7: 143,724,726-144,277,063 , GRCh38.p12 chr7|NW_018654714.1: 269,045-589,656 , TCAF1, 36 more genes
    nsv4679008copy number variation1nstd189human GRCh37.p13 chr7: 143,226,900-143,917,601 , GRCh38.p12 chr7: 143,529,807-144,220,508 , GRCh38.p12 chr7|NW_018654714.1: 149,171-589,656 , TCAF1, 37 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4663957copy number variation2nstd186human GRCh37 chr7: 143,248,293-143,563,494 , GRCh38.p12 chr7: 143,551,200-143,866,401 , GRCh38.p12 chr7|NW_018654714.1: 170,564-410,625 , RPL26P24, 13 more genes
    nsv4643269copy number variation3nstd186human GRCh37 chr7: 143,441,000-143,567,100 , GRCh38.p12 chr7: 143,743,907-143,870,007 , GRCh38.p12 chr7|NW_018654714.1: 288,227-414,232 TCAF1, LOC154761, 6 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