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 945

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 MIR484, NDE1, 37 more genes
    nsv7148105copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,475,455-16,308,356 , GRCh38.p12 chr16: 15,381,598-16,214,499 , GRCh38.p12 chr16|NT_187607.1: 1,039,549-1,872,496 NDE1, RPL15P20, 15 more genes
    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
    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
    nsv7094757copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,808,746-15,818,869 , GRCh38.p12 chr16: 15,714,889-15,725,012 , GRCh38.p12 chr16|NT_187607.1: 1,372,900-1,383,023 MYH11, NDE1
    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
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7076712inversion1nstd229human GRCh38 chr16: 15,435,384-15,663,982 , GRCh37.p13 chr16: 15,529,241-15,757,839 MIR484, MARF1, 4 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
    nsv7066617inversion1nstd229human GRCh38 chr16: 15,099,482-15,834,316 , GRCh37.p13 chr16: 15,193,339-15,928,173 MARF1, NDE1, 16 more genes
    nsv7059035inversion1nstd229human GRCh38 chr16: 15,565,040-16,913,283 , GRCh37.p13 chr16: 15,658,897-17,007,140 PKD1P2, MIR3179-2, 25 more genes
    nsv6978004copy number variation1nstd229human GRCh38 chr16: 15,672,242-15,677,318 , GRCh37.p13 chr16: 15,766,099-15,771,175 NDE1
    nsv6975644copy number variation1nstd229human GRCh38 chr16: 15,671,946-15,678,635 , GRCh37.p13 chr16: 15,765,803-15,772,492 NDE1
    nsv6975412copy number variation1nstd229human GRCh38 chr16: 15,692,212-15,698,272 , GRCh37.p13 chr16: 15,786,069-15,792,129 NDE1
    nsv6973044copy number variation1nstd229human GRCh38 chr16: 15,686,976-15,700,731 , GRCh37.p13 chr16: 15,780,833-15,794,588 NDE1
    nsv6971298copy number variation1nstd229human GRCh38 chr16: 15,722,101-15,734,500 , GRCh37.p13 chr16: 15,815,958-15,828,357 MYH11, NDE1
    nsv6967770copy number variation1nstd229human GRCh38 chr16: 15,712,965-15,713,607 , GRCh37.p13 chr16: 15,806,822-15,807,464 MYH11, NDE1
    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