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Items: 1 to 20 of 1055

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4728656copy number variation1nstd102humanLikely benign GRCh37 chr2: 43,457,560-43,554,972 , GRCh38.p12 chr2: 43,230,421-43,327,833 THADA
    nsv3876232copy number variation1nstd102humanLikely benign GRCh37 chr2: 43,518,750-43,602,889 , GRCh38.p12 chr2: 43,291,611-43,375,750 THADA
    nsv4728580copy number variation1nstd102humanLikely benign GRCh37 chr2: 43,489,278-43,559,950 , GRCh38.p12 chr2: 43,262,139-43,332,811 THADA
    nsv3877816copy number variation1nstd102humanBenign GRCh37 chr2: 43,496,986-43,555,506 , GRCh38.p12 chr2: 43,269,847-43,328,367 THADA
    nsv3890625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 43,495,260-43,528,441 , NCBI36 chr2: 43,348,764-43,381,945 , GRCh38 chr2: 43,268,121-43,301,302 THADA
    esv4006675copy number variation1estd231human GRCh37 chr2: 43,656,298-43,657,085 , GRCh38.p12 chr2: 43,429,159-43,429,946 THADA
    esv4006687copy number variation1estd231human GRCh37 chr2: 43,658,769-43,659,294 , GRCh38.p12 chr2: 43,431,630-43,432,155 THADA
    nsv6660149copy number variation1nstd229human GRCh38 chr2: 43,262,402-43,330,566 , GRCh37.p13 chr2: 43,489,541-43,557,705 THADA
    nsv6659624copy number variation1nstd229human GRCh38 chr2: 43,251,592-43,280,320 , GRCh37.p13 chr2: 43,478,731-43,507,459 THADA
    nsv6671192copy number variation1nstd229human GRCh38 chr2: 43,411,429-43,438,876 , GRCh37.p13 chr2: 43,638,568-43,666,015 THADA
    nsv6662724copy number variation1nstd229human GRCh38 chr2: 43,495,887-43,522,963 , GRCh37.p13 chr2: 43,723,026-43,750,102 THADA
    nsv6664864copy number variation1nstd229human GRCh38 chr2: 43,366,301-43,386,800 , GRCh37.p13 chr2: 43,593,440-43,613,939 THADA
    nsv6672151copy number variation1nstd229human GRCh38 chr2: 43,524,127-43,539,838 , GRCh37.p13 chr2: 43,751,266-43,766,977 THADA
    nsv6665969copy number variation1nstd229human GRCh38 chr2: 43,433,400-43,448,775 , GRCh37.p13 chr2: 43,660,539-43,675,914 THADA
    nsv6665703copy number variation1nstd229human GRCh38 chr2: 43,508,873-43,521,028 , GRCh37.p13 chr2: 43,736,012-43,748,167 THADA
    nsv6658560copy number variation1nstd229human GRCh38 chr2: 43,469,738-43,481,193 , GRCh37.p13 chr2: 43,696,877-43,708,332 THADA
    nsv6673966copy number variation1nstd229human GRCh38 chr2: 43,296,098-43,307,442 , GRCh37.p13 chr2: 43,523,237-43,534,581 THADA
    nsv6670013copy number variation1nstd229human GRCh38 chr2: 43,504,531-43,515,401 , GRCh37.p13 chr2: 43,731,670-43,742,540 THADA
    nsv6658908copy number variation1nstd229human GRCh38 chr2: 43,510,869-43,521,115 , GRCh37.p13 chr2: 43,738,008-43,748,254 THADA
    nsv6665315copy number variation1nstd229human GRCh38 chr2: 43,348,607-43,355,703 , GRCh37.p13 chr2: 43,575,746-43,582,842 THADA
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