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 119

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5971248insertion1nstd209human GRCh38 chr19: 50,369,558-50,369,558 , GRCh37.p13 chr19: 50,872,815-50,872,815 NAPSA, LOC105372437
    nsv5970571inversion1nstd209human GRCh38 chr19: 50,142,503-50,623,829 , GRCh37.p13 chr19: 50,645,760-51,127,086 KCNC3, MYBPC2, 16 more genes
    nsv5930647copy number variation1nstd209human GRCh38 chr19: 50,364,268-50,364,427 , GRCh37.p13 chr19: 50,867,525-50,867,684 LOC105372437, NAPSA
    nsv5524827copy number variation1nstd206human GRCh38 chr19: 50,365,143-50,365,251 , GRCh37.p13 chr19: 50,868,400-50,868,508 LOC105372437, NAPSA
    nsv5518054copy number variation1nstd206human GRCh38 chr19: 50,364,162-50,364,496 , GRCh37.p13 chr19: 50,867,419-50,867,753 NAPSA, LOC105372437
    nsv5323763copy number variation1nstd204human GRCh37.p13 chr19: 50,840,633-50,865,226 , GRCh38.p13 chr19: 50,337,376-50,361,969 NAPSA, NAPSB, 1 more genes
    nsv5296384copy number variation1nstd204human GRCh38.p13 chr19: 50,338,730-50,362,070 , GRCh37.p13 chr19: 50,841,987-50,865,327 NAPSB, NAPSA, 1 more genes
    nsv5293338copy number variation1nstd204human GRCh38.p13 chr19: 50,357,565-50,359,564 , GRCh37.p13 chr19: 50,860,822-50,862,821 LOC105372437, NAPSA
    nsv5289680copy number variation1nstd204human GRCh38.p13 chr19: 50,337,401-50,362,000 , GRCh37.p13 chr19: 50,840,658-50,865,257 NAPSA, LOC105372437, 1 more genes
    nsv5021039copy number variation1nstd200human GRCh38 chr19: 50,369,132-50,369,636 , GRCh37.p13 chr19: 50,872,389-50,872,893 LOC105372437, NAPSA
    nsv5021038copy number variation1nstd200human GRCh38 chr19: 50,364,612-50,365,295 , GRCh37.p13 chr19: 50,867,869-50,868,552 LOC105372437, NAPSA
    nsv4853375copy number variation1nstd200human GRCh37 chr19: 50,872,389-50,872,893 , GRCh38.p12 chr19: 50,369,132-50,369,636 NAPSA, LOC105372437
    nsv4853374copy number variation1nstd200human GRCh37 chr19: 50,868,400-50,868,508 , GRCh38.p12 chr19: 50,365,143-50,365,251 LOC105372437, NAPSA
    nsv4853372copy number variation1nstd200human GRCh37 chr19: 50,840,641-50,865,219 , GRCh38.p12 chr19: 50,337,384-50,361,962 LOC105372437, NAPSA, 1 more genes
    nsv4746093copy number variation1nstd199human GRCh37 chr19: 50,867,523-50,867,683 , GRCh38.p12 chr19: 50,364,266-50,364,426 NAPSA, LOC105372437
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676347copy number variation1nstd102humanUncertain significance GRCh37 chr19: 50,469,730-51,916,485 , GRCh38.p12 chr19: 49,966,473-51,413,231 VRK3, SYT3, 93 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