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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997078copy number variation1nstd229human GRCh38 chr17: 79,731,526-79,741,291 , GRCh37.p13 chr17|NW_003871089.1: 315,532-325,297 , GRCh37.p13 chr17: 77,705,288-77,715,090 ENPP7
    nsv6992563copy number variation1nstd229human GRCh38 chr17: 79,728,514-79,733,472 , GRCh37.p13 chr17|NW_003871089.1: 312,520-317,478 , GRCh37.p13 chr17: 77,702,276-77,707,270 ENPP7
    nsv6523597copy number variation1nstd223human GRCh38 chr17: 79,737,101-79,738,800 , GRCh37.p13 chr17: 77,710,900-77,712,599 , GRCh37.p13 chr17|NW_003871089.1: 321,107-322,806 ENPP7
    nsv5522047copy number variation1nstd206human GRCh38 chr17: 79,732,199-79,732,609 , GRCh37.p13 chr17: 77,705,997-77,706,407 , GRCh37.p13 chr17|NW_003871089.1: 316,205-316,615 ENPP7
    nsv6275398copy number variation1nstd214human GRCh38 chr17: 79,732,053-79,732,231 , GRCh37.p13 chr17|NW_003871089.1: 316,059-316,237 , GRCh37.p13 chr17: 77,705,815-77,706,029 ENPP7
    nsv5588076copy number variation1nstd207human GRCh38 chr17: 79,738,644-79,738,718 , GRCh37.p13 chr17: 77,712,443-77,712,517 , GRCh37.p13 chr17|NW_003871089.1: 322,650-322,724 ENPP7
    nsv5016964copy number variation1nstd200human GRCh38 chr17: 79,736,622-79,740,990 , GRCh37.p13 chr17|NW_003871089.1: 320,628-324,996 , GRCh37.p13 chr17: 77,710,421-77,714,789 ENPP7
    nsv4867440copy number variation1nstd200human GRCh37 chr17: 77,710,421-77,714,789 , GRCh38.p12 chr17: 79,736,622-79,740,990 ENPP7
    nsv5016963copy number variation1nstd200human GRCh38 chr17: 79,731,416-79,733,098 , GRCh37.p13 chr17|NW_003871089.1: 315,422-317,104 , GRCh37.p13 chr17: 77,705,178-77,706,896 ENPP7
    nsv4867441copy number variation1nstd200human GRCh37 chr17: 77,717,029-77,717,240 , GRCh38.p12 chr17: 79,743,230-79,743,441 ENPP7
    esv3210572copy number variation1estd209human GRCh37 chr17: 77,702,681-77,702,690 , GRCh38.p12 chr17: 79,728,919-79,728,928 ENPP7
    esv3210573copy number variation1estd209human GRCh37 chr17: 77,707,168-77,707,169 , GRCh38.p12 chr17: 79,733,370-79,733,371 ENPP7
    esv3210574copy number variation1estd209human GRCh37 chr17: 77,708,277-77,708,278 , GRCh38.p12 chr17: 79,734,479-79,734,479 ENPP7
    esv1079930copy number variation1estd22human NCBI36 chr17: 75,317,279-75,317,288 , GRCh37.p13 chr17|NW_003871089.1: 312,928-312,937 , GRCh37.p13 chr17: 77,702,684-77,702,693 , GRCh38.p12 chr17: 79,728,922-79,728,931 ENPP7
    esv1616822copy number variation1estd22human NCBI36 chr17: 75,324,965-75,324,969 , GRCh37.p13 chr17|NW_003871089.1: 320,577-320,581 , GRCh37.p13 chr17: 77,710,370-77,710,374 , GRCh38.p12 chr17: 79,736,571-79,736,575 ENPP7
    esv1125833copy number variation1estd22human NCBI36 chr17: 75,320,560-75,320,562 , GRCh37.p13 chr17|NW_003871089.1: 316,173-316,175 , GRCh37.p13 chr17: 77,705,965-77,705,967 , GRCh38.p12 chr17: 79,732,167-79,732,169 ENPP7
    esv1396222copy number variation1estd22human NCBI36 chr17: 75,322,888-75,322,889 , GRCh37.p13 chr17: 77,708,293-77,708,294 , GRCh37.p13 chr17|NW_003871089.1: 318,500-318,501 , GRCh38.p12 chr17: 79,734,494-79,734,495 ENPP7
    nsv106062copy number variation1nstd6human NCBI35 chr17: 75,322,888-75,322,889 , GRCh37.p13 chr17: 77,708,293-77,708,294 , GRCh37.p13 chr17|NW_003871089.1: 318,500-318,501 , GRCh38.p12 chr17: 79,734,494-79,734,495 ENPP7
    nsv4261230copy number variation1nstd166human GRCh37.p13 chr17: 77,707,659-77,708,137 , GRCh38.p12 chr17: 79,733,861-79,734,339 ENPP7
    nsv4619863copy number variation1nstd183human GRCh37 chr17: 77,698,597-77,704,447 , GRCh38.p12 chr17: 79,724,827-79,730,685 ENPP7
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