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 192

    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
    nsv5487170copy number variation1nstd206human GRCh38 chr7: 149,720,180-149,721,159 , GRCh37.p13 chr7: 149,417,271-149,418,250 KRBA1
    nsv5482543copy number variation1nstd206human GRCh38 chr7: 149,719,899-149,737,618 , GRCh37.p13 chr7: 149,416,990-149,434,707 KRBA1
    nsv5247636copy number variation1nstd204human GRCh38.p13 chr7: 149,730,401-149,737,300 , GRCh37.p13 chr7: 149,427,491-149,434,389 KRBA1
    nsv4951214copy number variation1nstd200human GRCh38 chr7: 149,658,512-149,722,959 , GRCh37.p13 chr7: 149,355,603-149,420,050 TRC-GCA21-1, TRC-GCA17-1, 2 more genes
    nsv4827293copy number variation1nstd200human GRCh37 chr7: 149,411,792-149,412,211 , GRCh38.p12 chr7: 149,714,701-149,715,120 KRBA1
    nsv4827290copy number variation1nstd200human GRCh37 chr7: 149,355,603-149,420,050 , GRCh38.p12 chr7: 149,658,512-149,722,959 TRC-GCA17-1, TRC-GCA21-1, 2 more genes
    nsv4729103copy number variation1nstd102humanUncertain significance GRCh37 chr7: 149,365,302-149,863,491 , GRCh38.p12 chr7: 149,668,211-150,166,402 SSPOP, TRC-GCA9-4, 8 more genes
    nsv4685723copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 CUL1, RNY1, 63 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
    nsv4680264copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,673,044 , GRCh38.p12 chr7: 149,665,479-149,975,955 SSPOP, KRBA1, 7 more genes
    nsv4680018copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,722,674 , GRCh38.p12 chr7: 149,665,479-150,025,585 SSPOP, KRBA1, 7 more genes
    nsv4679998copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,710,146 , GRCh38.p12 chr7: 149,665,479-150,013,057 SSPOP, KRBA1, 7 more genes
    nsv4678914copy number variation1nstd189human GRCh37.p13 chr7: 149,362,570-149,697,294 , GRCh38.p12 chr7: 149,665,479-150,000,205 SSPOP, KRBA1, 7 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
    nsv4675268copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017 ABCB8, THAP5P1, 237 more genes
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 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
    nsv4452353copy number variation1nstd102humannot provided GRCh37 chr7: 147,897,705-149,874,566 , GRCh38.p12 chr7: 148,200,613-150,177,477 RN7SL569P, ZNF746, 63 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