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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4920185copy number variation1nstd200human GRCh38 chr3: 132,595,284-132,637,709 , GRCh37.p13 chr3: 132,314,128-132,356,553 NPHP3-ACAD11, ACAD11, 1 more genes
    nsv4914773copy number variation1nstd200human GRCh38 chr3: 132,365,682-133,204,470 , GRCh37.p13 chr3: 132,084,526-132,923,314 NPHP3, ACKR4, 11 more genes
    nsv4791089copy number variation1nstd200human GRCh37 chr3: 132,314,128-132,356,553 , GRCh38.p12 chr3: 132,595,284-132,637,709 ACAD11, ACKR4, 1 more genes
    nsv4682381copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,184,839-132,441,199 , GRCh38.p12 chr3: 132,465,995-132,722,355 HSPA8P19, UBA5, 6 more genes
    nsv4596055copy number variation1nstd183human GRCh37 chr3: 131,866,636-132,504,231 , GRCh38.p12 chr3: 132,147,792-132,785,387 ACKR4, NPHP3-AS1, 15 more genes
    nsv4587244copy number variation1nstd183human GRCh37 chr3: 132,174,467-132,965,626 , GRCh38.p12 chr3: 132,455,623-133,246,782 TMEM108, NPHP3-AS1, 9 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 NPHP3-AS1, RNA5SP142, 218 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918871copy number variation1nstd102humanPathogenic GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861 FOXL2, NPHP3, 132 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 CLSTN2-AS1, COPB2, 177 more genes
    nsv3912335copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661 ACP3, FTH1P4, 130 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3883448copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,314,959-132,705,445 , GRCh38.p12 chr3: 132,596,115-132,986,601 NPHP3, NPHP3-AS1, 6 more genes
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