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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097750copy number variation1nstd102humanUncertain significance GRCh37 chr7: 65,546,770-65,557,899 , GRCh38.p12 chr7: 66,081,783-66,092,912 ASL
    nsv7097749copy number variation1nstd102humanUncertain significance GRCh37 chr7: 65,541,069-65,557,899 , GRCh38.p12 chr7: 66,076,082-66,092,912 ASL
    nsv7097383copy number variation1nstd102humanUncertain significance GRCh37 chr7: 65,551,562-65,557,909 , GRCh38.p12 chr7: 66,086,575-66,092,922 ASL
    nsv7097382copy number variation1nstd102humanPathogenic GRCh37 chr7: 65,547,857-65,548,171 , GRCh38.p12 chr7: 66,082,870-66,083,184 ASL
    nsv7049270inversion1nstd229human GRCh38 chr7: 66,055,057-66,105,679 , GRCh37.p13 chr7: 65,520,044-65,570,666 LOC644667, ASL
    nsv7048681inversion1nstd229human GRCh38 chr7: 65,849,741-66,368,250 , GRCh37.p13 chr7: 65,314,728-65,833,237 TPST1, GUSB, 9 more genes
    nsv7045287inversion1nstd229human GRCh38 chr7: 66,090,842-66,106,345 , GRCh37.p13 chr7: 65,555,829-65,571,332 ASL
    nsv7041738inversion1nstd229human GRCh38 chr7: 65,949,658-66,411,363 , GRCh37.p13 chr7: 65,414,645-65,876,350 ASL, GTF2IP9, 9 more genes
    nsv7041397inversion1nstd229human GRCh38 chr7: 65,600,026-71,276,703 , GRCh37.p13 chr7: 65,286,678-70,741,689 GALNT17, MTCO1P25, 74 more genes
    nsv6835608copy number variation1nstd229human GRCh38 chr7: 65,825,345-66,840,559 , GRCh37.p13 chr7: 65,290,332-66,305,546 LOC346329, RABGEF1P1, 27 more genes
    nsv6822868copy number variation1nstd229human GRCh38 chr7: 66,087,973-66,207,965 , GRCh37.p13 chr7: 65,552,960-65,672,952 ASL, TPST1, 1 more genes
    nsv6820869copy number variation1nstd229human GRCh38 chr7: 66,031,520-66,312,965 , GRCh37.p13 chr7: 65,496,507-65,777,952 LOC105375336, LOC644667, 3 more genes
    nsv6820566copy number variation1nstd229human GRCh38 chr7: 66,065,907-66,553,205 , GRCh37.p13 chr7: 65,530,894-66,018,192 LINC00174, RABGEF1P1, 12 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631988copy number variation1nstd224human GRCh37 chr7: 65,509,258-65,766,561 , GRCh38.p12 chr7: 66,044,271-66,301,574 LOC644667, ASL, 3 more genes
    nsv6618212copy number variation1nstd223human GRCh38 chr7: 66,084,902-66,085,804 , GRCh37.p13 chr7: 65,549,889-65,550,791 ASL
    nsv6614292copy number variation1nstd223human GRCh38 chr7: 66,074,569-66,079,110 , GRCh37.p13 chr7: 65,539,556-65,544,097 ASL
    nsv6609851copy number variation1nstd223human GRCh38 chr7: 66,085,284-66,098,126 , GRCh37.p13 chr7: 65,550,271-65,563,113 ASL
    nsv6606471copy number variation1nstd223human GRCh38 chr7: 66,078,945-66,102,377 , GRCh37.p13 chr7: 65,543,932-65,567,364 ASL
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
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