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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945651copy number variation1nstd209human GRCh38 chr17: 43,216,585-43,216,691 , GRCh37.p13 chr17: 41,368,604-41,368,710 TMEM106A
    nsv5936586copy number variation1nstd209human GRCh38 chr17: 43,212,392-43,213,017 , GRCh37.p13 chr17: 41,364,411-41,365,036 TMEM106A
    nsv5936437copy number variation1nstd209human GRCh38 chr17: 43,215,940-43,216,446 , GRCh37.p13 chr17: 41,367,959-41,368,465 TMEM106A
    nsv5928779copy number variation1nstd209human GRCh38 chr17: 43,217,312-43,217,679 , GRCh37.p13 chr17: 41,369,331-41,369,698 TMEM106A
    nsv5870677copy number variation1nstd209human GRCh38 chr17: 43,217,486-43,219,685 , GRCh37.p13 chr17: 41,369,505-41,371,704 CCDC200, TMEM106A
    nsv5868736copy number variation1nstd209human GRCh38 chr17: 43,214,837-43,216,136 , GRCh37.p13 chr17: 41,366,856-41,368,155 TMEM106A
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5289818copy number variation1nstd204human GRCh38.p13 chr17: 43,159,701-43,231,500 , GRCh37.p13 chr17: 41,311,718-41,383,489 CCDC200, LOC101929767, 3 more genes
    nsv5288617copy number variation1nstd204human GRCh38.p13 chr17: 43,204,704-43,215,136 , GRCh37.p13 chr17: 41,356,721-41,367,155 TMEM106A, NBR1
    nsv5288516copy number variation1nstd204human GRCh38.p13 chr17: 43,219,661-43,233,386 , GRCh37.p13 chr17: 41,371,680-41,383,489 TMEM106A, RNU2-1, 1 more genes
    nsv5287669copy number variation1nstd204human GRCh38.p13 chr17: 42,963,201-43,231,700 , GRCh37.p13 chr17: 41,115,218-41,383,489 PTGES3L, CCDC200, 15 more genes
    nsv5200272copy number variation1nstd205human GRCh37.p13 chr17: 41,242,185-41,378,464 , GRCh38.p12 chr17: 43,090,168-43,226,417 BRCA1, NBR1, 6 more genes
    nsv4729870copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,221,565-41,775,043 , GRCh38.p12 chr17: 43,069,548-43,697,675 LOC105371785, RNU6-406P, 24 more genes
    nsv4680708copy number variation1nstd189human GRCh37.p13 chr17: 41,357,686-42,167,307 , GRCh38.p12 chr17: 43,205,667-44,089,939 , ARL4D, 41 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4260262copy number variation1nstd166human GRCh37.p13 chr17: 41,364,413-41,365,037 , GRCh38.p12 chr17: 43,212,394-43,213,018 TMEM106A
    nsv3968801insertion1nstd168human GRCh37.p13 chr17: 41,368,996-41,509,271 , GRCh38 chr17: 43,216,977-43,431,903 ARL4D, RNU2-1, 7 more genes
    nsv3967439copy number variation1nstd168human GRCh38 chr17: 43,211,742-43,419,113 , GRCh37.p13 chr17: 41,363,761-41,496,481 RNU2-4P, LOC105371785, 8 more genes
    nsv3923117copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,080,123-43,897,875 , NCBI36 chr17: 38,485,666-39,330,769 , GRCh37 chr17: 41,232,140-41,975,243 RNU6-470P, CCDC200, 33 more genes
    nsv3922353copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,088,882-43,865,172 , GRCh37 chr17: 41,240,899-41,942,540 , NCBI36 chr17: 38,494,425-39,298,066 NBR1, LOC107985077, 31 more genes
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