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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6883588copy number variation1nstd229human GRCh38 chr10: 100,371,399-100,373,662 , GRCh37.p13 chr10: 102,131,156-102,133,419 OLMALINC
    nsv6883484copy number variation1nstd229human GRCh38 chr10: 100,383,498-100,385,897 , GRCh37.p13 chr10: 102,143,255-102,145,654 OLMALINC
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6441680copy number variation1nstd223human GRCh38 chr10: 99,317,365-100,480,706 , GRCh37.p13 chr10: 101,077,122-102,240,463 WNT8B, GOT1, 29 more genes
    nsv6132013copy number variation1nstd213human GRCh37 chr10: 101,250,000-103,200,001 , GRCh38.p12 chr10: 99,490,243-101,440,244 CHUK, ABCC2, 52 more genes
    nsv6131925copy number variation2nstd213human GRCh37 chr10: 101,250,000-103,190,001 , GRCh38.p12 chr10: 99,490,243-101,430,244 CHUK, ABCC2, 52 more genes
    nsv6131845copy number variation1nstd213human GRCh37 chr10: 100,150,000-103,440,001 , GRCh38.p12 chr10: 98,390,243-101,680,244 CHUK, ABCC2, 70 more genes
    nsv5909128copy number variation1nstd209human GRCh38 chr10: 100,374,012-100,381,214 , GRCh37.p13 chr10: 102,133,769-102,140,971 OLMALINC
    nsv5330320translocation1nstd200human GRCh37 chr10: 102,141,205-102,141,205 , GRCh37 chr10: 102,147,792-102,147,792 , GRCh38.p12 chr10: 100,388,035-100,388,035 , GRCh38.p12 chr10: 100,381,448-100,381,448 OLMALINC
    nsv4674975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,932,457-102,392,841 , GRCh38.p12 chr10: 100,172,700-100,633,084 NDUFB8, SNORA12, 12 more genes
    nsv4380194copy number variation1nstd173human GRCh37 chr10: 102,140,628-102,205,123 , GRCh38.p12 chr10: 100,380,871-100,445,366 OLMALINC
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4185321copy number variation1nstd166human GRCh37.p13 chr10: 102,143,255-102,145,650 , GRCh38.p12 chr10: 100,383,498-100,385,893 OLMALINC
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
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