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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5481664copy number variation1nstd206human GRCh38 chr7: 150,315,753-150,318,489 , GRCh37.p13 chr7: 150,012,842-150,015,578 ACTR3C, LRRC61
    nsv5476853copy number variation1nstd206human GRCh38 chr7: 150,312,212-150,318,259 , GRCh37.p13 chr7: 150,009,301-150,015,348 ACTR3C, LRRC61
    nsv5476425copy number variation1nstd206human GRCh38 chr7: 150,311,658-150,311,736 , GRCh37.p13 chr7: 150,008,747-150,008,825 LRRC61, ACTR3C
    nsv5305864copy number variation1nstd204human GRCh37.p13 chr7: 150,009,298-150,015,349 , GRCh38.p13 chr7: 150,312,209-150,318,260 ACTR3C, LRRC61
    nsv5252811copy number variation1nstd204human GRCh38.p13 chr7: 150,312,201-150,318,200 , GRCh37.p13 chr7: 150,009,290-150,015,289 ACTR3C, LRRC61
    nsv5247672copy number variation1nstd204human GRCh38.p13 chr7: 150,316,201-150,318,300 , GRCh37.p13 chr7: 150,013,290-150,015,389 ACTR3C, LRRC61
    nsv5243122copy number variation1nstd204human GRCh38.p13 chr7: 150,314,453-150,315,952 , GRCh37.p13 chr7: 150,011,542-150,013,041 LRRC61, ACTR3C
    nsv5242651copy number variation1nstd204human GRCh38.p13 chr7: 150,312,222-150,317,852 , GRCh37.p13 chr7: 150,009,311-150,014,941 ACTR3C, LRRC61
    nsv4951235copy number variation1nstd200human GRCh38 chr7: 150,319,355-150,319,451 , GRCh37.p13 chr7: 150,016,444-150,016,540 ACTR3C, LRRC61
    nsv4951234copy number variation1nstd200human GRCh38 chr7: 150,315,996-150,318,491 , GRCh37.p13 chr7: 150,013,085-150,015,580 LRRC61, ACTR3C
    nsv4951233copy number variation1nstd200human GRCh38 chr7: 150,312,212-150,318,259 , GRCh37.p13 chr7: 150,009,301-150,015,348 ACTR3C, LRRC61
    nsv4812419copy number variation1nstd200human GRCh37 chr7: 150,009,301-150,015,348 , GRCh38.p12 chr7: 150,312,212-150,318,259 LRRC61, ACTR3C
    nsv4754093inversion1nstd199human GRCh37 chr7: 149,731,009-153,760,532 , GRCh38.p12 chr7: 150,033,920-154,063,447 , AOC1, 98 more genes
    nsv4685715copy number variation1nstd102humannot provided GRCh37 chr7: 143,107,740-156,886,246 , GRCh38.p12 chr7: 143,410,647-157,093,552 CTAGE4, CDK5, 277 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4675268copy number variation1nstd102humanPathogenic GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017 ABCB8, THAP5P1, 237 more genes
    nsv4486433mobile element insertion1nstd166human GRCh37.p13 chr7: 150,019,799-150,019,799 , GRCh38.p12 chr7: 150,322,710-150,322,710 ACTR3C, LRRC61
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