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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7057364inversion1nstd229human GRCh38 chr7: 12,228,395-12,232,878 , GRCh37.p13 chr7: 12,268,021-12,272,504 TMEM106B
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7053494inversion1nstd229human GRCh38 chr7: 12,155,513-12,915,637 , GRCh37.p13 chr7: 12,195,139-12,955,262 SCIN, RN7SKP228, 13 more genes
    nsv7049984inversion1nstd229human GRCh38 chr7: 11,159,456-12,799,960 , GRCh37.p13 chr7: 11,199,083-12,839,585 THSD7A, LOC105375156, 17 more genes
    nsv7039999inversion1nstd229human GRCh38 chr7: 11,885,399-12,345,655 , GRCh37.p13 chr7: 11,925,025-12,385,281 TMEM106B, VWDE
    nsv6817863copy number variation1nstd229human GRCh38 chr7: 12,235,916-12,264,596 , GRCh37.p13 chr7: 12,275,542-12,304,222 TMEM106B
    nsv6817070copy number variation1nstd229human GRCh38 chr7: 12,189,887-12,265,621 , GRCh37.p13 chr7: 12,229,513-12,305,247 TMEM106B
    nsv6815967copy number variation1nstd229human GRCh38 chr7: 12,201,101-12,212,400 , GRCh37.p13 chr7: 12,240,727-12,252,026 TMEM106B
    nsv6811891copy number variation1nstd229human GRCh38 chr7: 12,235,642-12,287,524 , GRCh37.p13 chr7: 12,275,268-12,327,150 TMEM106B
    nsv6810907copy number variation1nstd229human GRCh38 chr7: 11,465,438-12,452,163 , GRCh37.p13 chr7: 11,505,065-12,491,789 LOC105375155, TMEM106B, 6 more genes
    nsv6809645copy number variation1nstd229human GRCh38 chr7: 11,932,975-12,219,837 , GRCh37.p13 chr7: 11,972,601-12,259,463 TMEM106B
    nsv6809190copy number variation1nstd229human GRCh38 chr7: 12,242,085-12,242,399 , GRCh37.p13 chr7: 12,281,711-12,282,025 TMEM106B
    nsv6809042copy number variation1nstd229human GRCh38 chr7: 12,022,267-12,209,808 , GRCh37.p13 chr7: 12,061,893-12,249,434 TMEM106B
    nsv6808736copy number variation1nstd229human GRCh38 chr7: 12,230,621-12,231,521 , GRCh37.p13 chr7: 12,270,247-12,271,147 TMEM106B
    nsv6806310copy number variation1nstd229human GRCh38 chr7: 12,212,612-12,214,068 , GRCh37.p13 chr7: 12,252,238-12,253,694 TMEM106B
    nsv6805962copy number variation1nstd229human GRCh38 chr7: 12,226,401-12,317,700 , GRCh37.p13 chr7: 12,266,027-12,357,326 TMEM106B
    nsv6805090copy number variation1nstd229human GRCh38 chr7: 11,673,765-12,709,856 , GRCh37.p13 chr7: 11,713,392-12,749,481 TAS2R2P, LOC105375155, 14 more genes
    nsv6804348copy number variation1nstd229human GRCh38 chr7: 12,237,692-12,244,538 , GRCh37.p13 chr7: 12,277,318-12,284,164 TMEM106B
    nsv6798747copy number variation1nstd229human GRCh38 chr7: 12,234,676-12,239,167 , GRCh37.p13 chr7: 12,274,302-12,278,793 TMEM106B
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