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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097542copy number variation1nstd102humanPathogenic GRCh37 chr5: 70,892,087-70,892,211 , GRCh38.p12 chr5|NT_187651.1: 1,126,235-1,126,359 , GRCh38.p12 chr5|NW_003315917.2: 1,594,745-1,594,869 , GRCh38.p12 chr5: 71,596,260-71,596,384 MCCC2
    nsv7097289copy number variation1nstd102humanPathogenic GRCh37 chr5: 70,898,323-70,900,305 , GRCh38.p12 chr5: 71,602,496-71,604,478 , GRCh38.p12 chr5|NT_187651.1: 1,132,471-1,134,453 , GRCh38.p12 chr5|NW_003315917.2: 1,600,981-1,602,963 MCCC2
    nsv7097288copy number variation1nstd102humanPathogenic GRCh37 chr5: 70,895,476-70,900,305 , GRCh38.p12 chr5: 71,599,649-71,604,478 , GRCh38.p12 chr5|NT_187651.1: 1,129,624-1,134,453 , GRCh38.p12 chr5|NW_003315917.2: 1,598,134-1,602,963 MCCC2
    nsv7097158copy number variation1nstd102humanPathogenic GRCh37 chr5: 70,930,773-70,930,871 , GRCh38.p12 chr5: 71,634,946-71,635,044 MCCC2
    nsv7096785copy number variation1nstd102humanUncertain significance GRCh37 chr5: 70,808,992-70,952,687 , GRCh38.p12 chr5: 71,513,165-71,656,860 , GRCh38.p12 chr5|NT_187651.1: 1,043,140-1,144,418 , GRCh38.p12 chr5|NW_003315917.2: 1,511,650-1,612,928 HMGN1P12, BDP1, 1 more genes
    nsv7055630inversion1nstd229human GRCh38 chr5: 66,647,773-71,648,116 , GRCh37.p13 chr5: 65,943,601-70,943,943 OCLNP1, CDK7, 96 more genes
    nsv6775046copy number variation1nstd229human GRCh38 chr5: 71,653,301-71,656,400 , GRCh37.p13 chr5: 70,949,128-70,952,227 MCCC2
    nsv6773551copy number variation1nstd229human GRCh38 chr5: 71,618,901-71,649,300 , GRCh37.p13 chr5: 70,914,728-70,945,127 MCCC2
    nsv6772207copy number variation1nstd229human GRCh38 chr5: 71,617,140-71,617,364 , GRCh37.p13 chr5: 70,912,967-70,913,191 MCCC2
    nsv6771182copy number variation1nstd229human GRCh38 chr5: 71,619,687-71,620,073 , GRCh37.p13 chr5: 70,915,514-70,915,900 MCCC2
    nsv6768485copy number variation1nstd229human GRCh38 chr5: 71,628,999-71,648,277 , GRCh37.p13 chr5: 70,924,826-70,944,104 MCCC2
    nsv6768079copy number variation1nstd229human GRCh38 chr5: 71,638,473-71,638,539 , GRCh37.p13 chr5: 70,934,300-70,934,366 MCCC2
    nsv6768062copy number variation1nstd229human GRCh38 chr5: 71,627,171-71,627,641 , GRCh37.p13 chr5: 70,922,998-70,923,468 MCCC2
    nsv6765691copy number variation1nstd229human GRCh38 chr5: 71,615,370-71,624,207 , GRCh37.p13 chr5: 70,911,197-70,920,034 MCCC2
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6762763copy number variation1nstd229human GRCh38 chr5: 71,611,378-71,611,539 , GRCh37.p13 chr5: 70,907,205-70,907,366 MCCC2
    nsv6759917copy number variation1nstd229human GRCh38 chr5: 71,642,435-71,653,313 , GRCh37.p13 chr5: 70,938,262-70,949,140 MCCC2
    nsv6758948copy number variation1nstd229human GRCh38 chr5: 71,628,052-71,637,808 , GRCh37.p13 chr5: 70,923,879-70,933,635 MCCC2
    nsv6630794copy number variation1nstd224human GRCh37 chr5: 70,939,675-70,952,652 , GRCh38.p12 chr5: 71,643,848-71,656,825 MCCC2
    nsv6630793copy number variation1nstd224human GRCh37 chr5: 70,922,543-70,945,029 , GRCh38.p12 chr5: 71,626,716-71,649,202 MCCC2
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