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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938426copy number variation1nstd209human GRCh38 chr13: 103,031,462-103,049,960 , GRCh37.p13 chr13: 103,683,812-103,702,310 SLC10A2
    nsv5865402copy number variation1nstd209human GRCh38 chr13: 103,036,554-103,043,153 , GRCh37.p13 chr13: 103,688,904-103,695,503 SLC10A2
    nsv5863032copy number variation1nstd209human GRCh38 chr13: 103,047,207-103,049,295 , GRCh37.p13 chr13: 103,699,557-103,701,645 SLC10A2
    nsv5859587copy number variation1nstd209human GRCh38 chr13: 103,031,489-103,043,453 , GRCh37.p13 chr13: 103,683,839-103,695,803 SLC10A2
    nsv5713231mobile element insertion1nstd211human GRCh38 chr13: 103,045,770-103,045,770 , GRCh37.p13 chr13: 103,698,120-103,698,120 SLC10A2
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5510834copy number variation1nstd206human GRCh38 chr13: 103,054,058-103,054,541 , GRCh37.p13 chr13: 103,706,408-103,706,891 SLC10A2
    nsv5507245copy number variation1nstd206human GRCh38 chr13: 103,031,462-103,049,964 , GRCh37.p13 chr13: 103,683,812-103,702,314 SLC10A2
    nsv5500740copy number variation1nstd206human GRCh38 chr13: 103,059,885-103,069,423 , GRCh37.p13 chr13: 103,712,235-103,721,773 SLC10A2
    nsv5498368copy number variation1nstd206human GRCh38 chr13: 103,059,373-103,060,113 , GRCh37.p13 chr13: 103,711,723-103,712,463 SLC10A2
    nsv5419230mobile element insertion1nstd206human GRCh38 chr13: 103,045,770-103,045,821 , GRCh37.p13 chr13: 103,698,120-103,698,171 SLC10A2
    nsv5348918translocation1nstd200human GRCh38 chr13: 103,059,373-103,059,373 , GRCh38 chr13: 103,060,113-103,060,113 , GRCh37.p13 chr13: 103,711,723-103,711,723 , GRCh37.p13 chr13: 103,712,463-103,712,463 SLC10A2
    nsv5345706translocation1nstd200human GRCh37 chr13: 103,711,723-103,711,723 , GRCh37 chr13: 103,712,463-103,712,463 , GRCh38.p12 chr13: 103,059,373-103,059,373 , GRCh38.p12 chr13: 103,060,113-103,060,113 SLC10A2
    nsv5319726copy number variation1nstd204human GRCh38.p13 chr13: 103,031,460-103,049,965 , GRCh37.p13 chr13: 103,683,810-103,702,315 SLC10A2
    nsv5271374copy number variation1nstd204human GRCh38.p13 chr13: 103,031,501-103,050,700 , GRCh37.p13 chr13: 103,683,851-103,703,050 SLC10A2
    nsv5268165copy number variation1nstd204human GRCh38.p13 chr13: 103,029,351-103,043,706 , GRCh37.p13 chr13: 103,681,701-103,696,056 SLC10A2
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4998517copy number variation1nstd200human GRCh38 chr13: 103,059,885-103,069,423 , GRCh37.p13 chr13: 103,712,235-103,721,773 SLC10A2
    nsv4998516copy number variation1nstd200human GRCh38 chr13: 103,043,462-103,052,512 , GRCh37.p13 chr13: 103,695,812-103,704,862 SLC10A2
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