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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5463215copy number variation1nstd206human GRCh38 chr7: 15,681,832-15,681,905 , GRCh37.p13 chr7: 15,721,457-15,721,530 LOC105375166, MEOX2
    nsv5223878copy number variation1nstd204human GRCh38.p13 chr7: 15,678,801-15,683,600 , GRCh37.p13 chr7: 15,718,426-15,723,225 MEOX2, LOC105375166
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4826677copy number variation1nstd200human GRCh37 chr7: 15,700,636-15,706,885 , GRCh38.p12 chr7: 15,661,011-15,667,260 MEOX2, LOC105375166
    nsv4768371copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542 HDAC9, LOC101927668, 60 more genes
    nsv4674987copy number variation1nstd102humanPathogenic GRCh37 chr7: 13,886,653-20,267,202 , GRCh38.p12 chr7: 13,847,028-20,227,579 BZW2, LOC105375168, 64 more genes
    nsv4609178copy number variation1nstd183human GRCh37 chr7: 15,698,178-15,718,464 , GRCh38.p12 chr7: 15,658,553-15,678,839 MEOX2, LOC105375166
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4455587copy number variation1nstd102humanUncertain significance GRCh37 chr7: 15,586,378-16,252,720 , GRCh38.p12 chr7: 15,546,753-16,213,095 LOC105375166, CRPPA, 8 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4149983copy number variation1nstd166human GRCh37.p13 chr7: 15,700,621-15,706,884 , GRCh38.p12 chr7: 15,660,996-15,667,259 LOC105375166, MEOX2
    nsv3923125copy number variation1nstd102humanPathogenic GRCh38 chr7: 11,122,492-16,479,303 , NCBI36 chr7: 11,128,644-16,485,453 , GRCh37 chr7: 11,162,119-16,518,928 THRAP3P3, ETV1, 43 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 LOC401312, IQCE, 411 more genes
    nsv3922284copy number variation1nstd102humanLikely benign NCBI36 chr7: 15,539,962-15,861,819 , GRCh37 chr7: 15,573,437-15,895,294 , GRCh38 chr7: 15,533,812-15,855,669 MEOX2, AGMO, 5 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 MMD2, ICA1-AS1, 554 more genes
    nsv3916683copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634 ZNF12, LOC105375183, 389 more genes
    nsv3916518copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,737,760-27,246,914 , NCBI36 chr7: 1,704,286-27,213,439 , GRCh38 chr7: 1,698,124-27,207,295 LOC105375156, LOC105375133, 365 more genes
    nsv3915802copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008 RPL23AP52, IQCE, 638 more genes
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