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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951476insertion1nstd209human GRCh38 chr5: 138,553,611-138,553,611 , GRCh37.p13 chr5: 137,889,300-137,889,300 HSPA9
    nsv5892800copy number variation1nstd209human GRCh38 chr5: 138,553,442-138,553,588 , GRCh37.p13 chr5: 137,889,131-137,889,277 HSPA9
    nsv5721675mobile element insertion1nstd211human GRCh38 chr5: 138,571,976-138,571,976 , GRCh37.p13 chr5: 137,907,665-137,907,665 LOC105379193, HSPA9
    nsv5715335mobile element insertion1nstd211human GRCh38 chr5: 138,572,247-138,572,247 , GRCh37.p13 chr5: 137,907,936-137,907,936 HSPA9, LOC105379193
    nsv5643296insertion1nstd207human GRCh38 chr5: 138,572,247-138,572,247 , GRCh37.p13 chr5: 137,907,936-137,907,936 HSPA9, LOC105379193
    nsv5563220mobile element insertion1nstd206human GRCh38 chr5: 138,572,262-138,572,298 , GRCh37.p13 chr5: 137,907,951-137,907,987 HSPA9, LOC105379193
    nsv5461638copy number variation1nstd206human GRCh38 chr5: 138,553,772-138,553,856 , GRCh37.p13 chr5: 137,889,461-137,889,545 HSPA9
    nsv5461435copy number variation1nstd206human GRCh38 chr5: 138,556,116-138,556,451 , GRCh37.p13 chr5: 137,891,805-137,892,140 HSPA9
    nsv5460572copy number variation1nstd206human GRCh38 chr5: 138,561,818-138,562,492 , GRCh37.p13 chr5: 137,897,507-137,898,181 HSPA9
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5368972translocation1nstd200human GRCh38 chr12: 4,575,070-4,575,070 , GRCh38 chr5: 138,555,339-138,555,339 , GRCh37.p13 chr12: 4,684,236-4,684,236 , GRCh37.p13 chr5: 137,891,028-137,891,028 HSPA9, DYRK4
    nsv5302987copy number variation1nstd204human GRCh37.p13 chr5: 137,897,686-137,905,656 , GRCh38.p13 chr5: 138,561,997-138,569,967 LOC105379193, HSPA9
    nsv5227204copy number variation1nstd204human GRCh38.p13 chr5: 138,562,248-138,563,299 , GRCh37.p13 chr5: 137,897,937-137,898,988 HSPA9
    nsv5223079copy number variation1nstd204human GRCh38.p13 chr5: 138,561,569-138,569,918 , GRCh37.p13 chr5: 137,897,258-137,905,607 LOC105379193, SNORD63, 1 more genes
    nsv5199684mobile element insertion1nstd203human GRCh38 chr5: 138,572,252-138,572,252 , GRCh37.p13 chr5: 137,907,941-137,907,941 HSPA9, LOC105379193
    nsv5192310mobile element insertion1nstd203human GRCh38 chr5: 138,572,250-138,572,250 , GRCh37.p13 chr5: 137,907,939-137,907,939 HSPA9, LOC105379193
    nsv5187917mobile element insertion1nstd203human GRCh38 chr5: 138,572,251-138,572,251 , GRCh37.p13 chr5: 137,907,940-137,907,940 HSPA9, LOC105379193
    nsv5187079mobile element insertion1nstd203human GRCh38 chr5: 138,572,247-138,572,247 , GRCh37.p13 chr5: 137,907,936-137,907,936 LOC105379193, HSPA9
    nsv5186464mobile element insertion1nstd203human GRCh38 chr5: 138,572,248-138,572,248 , GRCh37.p13 chr5: 137,907,937-137,907,937 LOC105379193, HSPA9
    nsv5181842mobile element insertion1nstd203human GRCh38 chr5: 138,571,976-138,571,976 , GRCh37.p13 chr5: 137,907,665-137,907,665 HSPA9, LOC105379193
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