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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948442insertion1nstd209human GRCh38 chr10: 87,798,625-87,798,625 , GRCh37.p13 chr10: 89,558,382-89,558,382 ATAD1
    nsv5914952copy number variation1nstd209human GRCh38 chr10: 87,839,787-87,839,836 , GRCh37.p13 chr10: 89,599,544-89,599,593 ATAD1, CFL1P1
    nsv5912903copy number variation1nstd209human GRCh38 chr10: 87,801,483-87,801,540 , GRCh37.p13 chr10: 89,561,240-89,561,297 ATAD1
    nsv5672610copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,683,123-89,725,321 , GRCh38.p12 chr10: 86,923,366-87,965,564 FAM245A, BMPR1A, 30 more genes
    nsv5628733insertion1nstd207human GRCh38 chr10: 87,824,129-87,824,129 , GRCh37.p13 chr10: 89,583,886-89,583,886 CFL1P1, ATAD1
    nsv5592172copy number variation1nstd207human GRCh38 chr10: 87,839,787-87,839,836 , GRCh37.p13 chr10: 89,599,544-89,599,593 CFL1P1, ATAD1
    nsv5589702copy number variation1nstd207human GRCh38 chr10: 87,801,483-87,801,540 , GRCh37.p13 chr10: 89,561,240-89,561,297 ATAD1
    nsv5491416copy number variation1nstd206human GRCh38 chr10: 87,828,415-87,828,539 , GRCh37.p13 chr10: 89,588,172-89,588,296 ATAD1, CFL1P1
    nsv5484877copy number variation1nstd206human GRCh38 chr10: 87,840,380-87,842,984 , GRCh37.p13 chr10: 89,600,137-89,602,741 ATAD1, CFL1P1
    nsv5479295copy number variation1nstd206human GRCh38 chr10: 87,747,629-87,749,576 , GRCh37.p13 chr10: 89,507,386-89,509,333 ATAD1, PAPSS2
    nsv5478477copy number variation1nstd206human GRCh38 chr10: 87,839,787-87,839,837 , GRCh37.p13 chr10: 89,599,544-89,599,594 ATAD1, CFL1P1
    nsv5347956translocation1nstd200human GRCh38 chr10: 87,800,188-87,800,188 , GRCh38 chr10: 87,800,373-87,800,373 , GRCh37.p13 chr10: 89,560,130-89,560,130 , GRCh37.p13 chr10: 89,559,945-89,559,945 ATAD1
    nsv5347955translocation1nstd200human GRCh38 chr10: 87,749,576-87,749,576 , GRCh38 chr10: 87,747,629-87,747,629 , GRCh37.p13 chr10: 89,507,386-89,507,386 , GRCh37.p13 chr10: 89,509,333-89,509,333 PAPSS2, ATAD1
    nsv5333276translocation1nstd200human GRCh37 chr10: 89,574,915-89,574,915 , GRCh37 chr10: 89,574,851-89,574,851 , GRCh38.p12 chr10: 87,815,158-87,815,158 , GRCh38.p12 chr10|NW_013171807.1: 30,916-30,916 , GRCh38.p12 chr10: 87,815,094-87,815,094 , GRCh38.p12 chr10|NW_013171807.1: 30,980-30,980 ATAD1
    nsv5321407translocation1nstd204human GRCh38.p13 chr10: 87,800,188-87,800,188 , GRCh38.p13 chr10: 87,800,373-87,800,373 , GRCh37.p13 chr10: 89,559,945-89,559,945 , GRCh37.p13 chr10: 89,560,130-89,560,130 ATAD1
    nsv5242231copy number variation1nstd204human GRCh38.p13 chr10: 87,818,171-87,819,270 , GRCh37.p13 chr10: 89,577,928-89,579,027 ATAD1, CFL1P1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986539copy number variation1nstd200human GRCh38 chr10: 87,820,514-87,823,257 , GRCh37.p13 chr10: 89,580,271-89,583,014 ATAD1, CFL1P1
    nsv4986538copy number variation1nstd200human GRCh38 chr10: 87,815,094-87,815,158 , GRCh37.p13 chr10: 89,574,851-89,574,915 ATAD1
    nsv4986537copy number variation1nstd200human GRCh38 chr10: 87,758,529-87,773,779 , GRCh37.p13 chr10: 89,518,286-89,533,536 ATAD1
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