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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893657copy number variation1nstd209human GRCh38 chr5: 54,534,587-54,534,693 , GRCh37.p13 chr5: 53,830,417-53,830,523 SNX18
    nsv5843089copy number variation1nstd209human GRCh38 chr5: 54,568,824-54,575,032 , GRCh37.p13 chr5: 53,864,654-53,870,862 SNX18
    nsv5723390mobile element insertion1nstd211human GRCh38 chr5: 54,538,591-54,538,591 , GRCh37.p13 chr5: 53,834,421-53,834,421 SNX18
    nsv5675681mobile element insertion1nstd211human GRCh38 chr5: 54,535,198-54,535,198 , GRCh37.p13 chr5: 53,831,028-53,831,028 SNX18
    nsv5576862copy number variation1nstd207human GRCh38 chr5: 54,534,612-54,534,718 , GRCh37.p13 chr5: 53,830,442-53,830,548 SNX18
    nsv5460585copy number variation1nstd206human GRCh38 chr5: 54,575,508-54,576,981 , GRCh37.p13 chr5: 53,871,338-53,872,811 SNX18
    nsv5399692mobile element insertion1nstd206human GRCh38 chr5: 54,535,198-54,535,249 , GRCh37.p13 chr5: 53,831,028-53,831,079 SNX18
    nsv5368393translocation1nstd200human GRCh38 chr5: 54,567,766-54,567,766 , GRCh38 chr5: 54,571,236-54,571,236 , GRCh37.p13 chr5: 53,867,066-53,867,066 , GRCh37.p13 chr5: 53,863,596-53,863,596 SNX18
    nsv5331791translocation1nstd200human GRCh37 chr5: 53,867,066-53,867,066 , GRCh37 chr5: 53,863,596-53,863,596 , GRCh38.p12 chr5: 54,571,236-54,571,236 , GRCh38.p12 chr5: 54,567,766-54,567,766 SNX18
    nsv5223753copy number variation1nstd204human GRCh38.p13 chr5: 54,569,699-54,575,032 , GRCh37.p13 chr5: 53,865,529-53,870,862 SNX18
    nsv5195272mobile element insertion1nstd203human GRCh38 chr5: 54,538,591-54,538,596 , GRCh37.p13 chr5: 53,834,421-53,834,426 SNX18
    nsv5083039mobile element insertion1nstd203human GRCh38 chr5: 54,616,768-54,616,784 , GRCh37.p13 chr5: 53,912,598-53,912,614 SNX18
    nsv4931565copy number variation1nstd200human GRCh38 chr5: 54,571,235-54,574,674 , GRCh37.p13 chr5: 53,867,065-53,870,504 SNX18
    nsv4931564copy number variation1nstd200human GRCh38 chr5: 54,524,482-54,524,621 , GRCh37.p13 chr5: 53,820,312-53,820,451 SNX18
    nsv4931563copy number variation1nstd200human GRCh38 chr5: 54,517,702-54,517,788 , GRCh37.p13 chr5: 53,813,532-53,813,618 SNX18
    nsv4679914copy number variation1nstd189human GRCh37.p13 chr5: 53,271,306-53,916,293 , GRCh38.p12 chr5: 53,975,476-54,620,463 , HSPB3, 5 more genes
    nsv4598156copy number variation1nstd183human GRCh37 chr5: 53,818,527-53,819,228 , GRCh38.p12 chr5: 54,522,697-54,523,398 SNX18
    nsv4568427mobile element insertion1nstd166human GRCh37.p13 chr5: 53,834,421-53,834,421 , GRCh38.p12 chr5: 54,538,591-54,538,591 SNX18
    nsv4478334mobile element insertion1nstd166human GRCh37.p13 chr5: 53,889,535-53,889,535 , GRCh38.p12 chr5: 54,593,705-54,593,705 SNX18
    nsv4457059copy number variation1nstd102humanUncertain significance GRCh37 chr5: 53,263,426-53,916,242 , GRCh38.p12 chr5: 53,967,596-54,620,412 RN7SL801P, ARL15, 4 more genes
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