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Items: 1 to 20 of 128

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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
    nsv5470684copy number variation1nstd206human GRCh38 chr7: 18,900,649-18,903,683 , GRCh37.p13 chr7: 18,940,272-18,943,306 HDAC9, HDAC9-AS1
    nsv5110279mobile element insertion1nstd203human GRCh38 chr7: 18,889,219-18,889,233 , GRCh37.p13 chr7: 18,928,842-18,928,856 HDAC9-AS1, HDAC9
    nsv4955829copy number variation1nstd200human GRCh38 chr7: 18,900,649-18,903,683 , GRCh37.p13 chr7: 18,940,272-18,943,306 HDAC9-AS1, HDAC9
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4826766copy number variation1nstd200human GRCh37 chr7: 18,940,272-18,943,306 , GRCh38.p12 chr7: 18,900,649-18,903,683 HDAC9, HDAC9-AS1
    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
    nsv4682307copy number variation1nstd102humanUncertain significance GRCh37 chr7: 18,330,087-18,975,565 , GRCh38.p12 chr7: 18,290,464-18,935,942 HDAC9, RN7SKP266, 2 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
    nsv4612817copy number variation1nstd183human GRCh37 chr7: 18,935,865-18,952,075 , GRCh38.p12 chr7: 18,896,242-18,912,452 HDAC9-AS1, HDAC9
    nsv4489833mobile element insertion1nstd166human GRCh37.p13 chr7: 18,941,381-18,941,381 , GRCh38.p12 chr7: 18,901,758-18,901,758 HDAC9-AS1, HDAC9
    nsv4482899mobile element insertion1nstd166human GRCh37.p13 chr7: 18,928,842-18,928,842 , GRCh38.p12 chr7: 18,889,219-18,889,219 HDAC9, HDAC9-AS1
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 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
    nsv4143096copy number variation1nstd166human GRCh37.p13 chr7: 18,929,061-18,930,072 , GRCh38.p12 chr7: 18,889,438-18,890,449 HDAC9, HDAC9-AS1
    nsv4138766copy number variation1nstd166human GRCh37.p13 chr7: 18,940,309-18,940,844 , GRCh38.p12 chr7: 18,900,686-18,901,221 HDAC9, HDAC9-AS1
    nsv4138483copy number variation1nstd166human GRCh37.p13 chr7: 18,927,048-18,935,210 , GRCh38.p12 chr7: 18,887,425-18,895,587 HDAC9-AS1, HDAC9
    nsv4137305copy number variation1nstd166human GRCh37.p13 chr7: 18,925,556-18,931,673 , GRCh38.p12 chr7: 18,885,933-18,892,050 HDAC9-AS1, HDAC9
    nsv3922488copy number variation1nstd102humanPathogenic GRCh37 chr7: 16,161,141-20,647,522 , GRCh38 chr7: 16,121,516-20,607,899 , NCBI36 chr7: 16,127,666-20,614,047 HDAC9, LOC105375168, 53 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
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