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 710

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148099copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,125,542-16,388,672 , GRCh38.p12 chr16: 15,031,685-16,294,815 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,952,820 LOC100505915, ABCC1, 28 more genes
    nsv7148091copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,853,752-16,666,672 , GRCh38.p12 chr16: 14,759,895-16,572,815 RPL17P40, PKD1P3-NPIPA1, 54 more genes
    nsv7147255copy number variation1nstd232human GRCh38.p12 chr16: 15,104,404-15,104,542 , GRCh37.p13 chr16: 15,198,261-15,198,399 PDXDC1, LOC100505915, 2 more genes
    nsv7141046copy number variation1nstd232human GRCh38.p12 chr16: 15,104,429-15,104,542 , GRCh37.p13 chr16: 15,198,286-15,198,399 PDXDC1, LOC100505915, 2 more genes
    nsv7139638copy number variation1nstd232human GRCh38.p12 chr16: 15,104,403-15,104,473 , GRCh37.p13 chr16: 15,198,260-15,198,330 , GRCh38.p12 chr16|NT_187607.1: 565,202-565,269 PDXDC1, LOC100505915, 2 more genes
    nsv7137121copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,819,740-16,364,041 , GRCh38.p12 chr16: 14,725,883-16,270,184 , GRCh38.p12 chr16|NT_187607.1: 266,171-1,928,187 ABCC6, ABCC1, 54 more genes
    nsv7099031copy number variation1nstd102humanUncertain significance GRCh38 chr16: 14,683,149-16,205,174 , GRCh37.p13 chr16: 14,777,006-16,299,031 LOC100288162, LOC105371096, 43 more genes
    nsv7098843copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 14,683,149-16,536,956 , GRCh37.p13 chr16: 14,777,006-16,630,813 ABCC6, ABCC1, 56 more genes
    nsv7093396copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,927,709-16,484,731 , GRCh38.p12 chr16: 14,833,852-16,390,874 ABCC6, ABCC1, 50 more genes
    nsv7076232inversion1nstd229human GRCh38 chr16: 14,972,012-15,457,502 , GRCh37.p13 chr16: 15,065,869-15,551,359 MIR3180-4, LOC105371097, 14 more genes
    nsv7068744inversion1nstd229human GRCh38 chr16: 14,595,692-15,383,928 , GRCh37.p13 chr16: 14,689,549-15,477,785 PKD1P6, NPIPA5, 32 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7067385inversion1nstd229human GRCh38 chr16: 15,051,408-15,524,165 , GRCh37.p13 chr16: 15,145,265-15,618,022 LOC105371096, MPV17L, 13 more genes
    nsv7066617inversion1nstd229human GRCh38 chr16: 15,099,482-15,834,316 , GRCh37.p13 chr16: 15,193,339-15,928,173 MARF1, NDE1, 16 more genes
    nsv7065280inversion1nstd229human GRCh38 chr16: 14,489,001-15,167,857 , GRCh37.p13 chr16: 14,582,858-15,261,714 NPIPA2, PARN, 31 more genes
    nsv6967585copy number variation1nstd229human GRCh38 chr16: 14,928,133-16,326,551 , GRCh37.p13 chr16: 15,021,990-16,420,408 NPIPA5, PKD1P6, 39 more genes
    nsv6637929copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,780,544-16,330,627 , GRCh38.p12 chr16: 14,686,687-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 259,546-1,894,768 LOC102724984, ABCC6P2, 54 more genes
    nsv6637792copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,925,995-16,309,165 , GRCh38.p12 chr16: 14,832,138-16,215,308 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,873,305 ABCC6, ABCC1, 49 more genes
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center