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Items: 1 to 20 of 981

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128887copy number variation1nstd186human GRCh37 chr21: 45,950,129-45,950,247 , GRCh38.p12 chr21: 44,530,246-44,530,364 TSPEAR
    nsv6117180mobile element insertion1nstd186human GRCh37 chr21: 46,094,190-46,094,241 , GRCh38.p12 chr21: 44,674,273-44,674,324 TSPEAR, IMMTP1
    nsv5978189inversion1nstd209human GRCh38 chr21: 44,550,659-44,628,117 , GRCh37.p13 chr21: 45,970,542-46,048,034 , GRCh37.p13 chr21|NW_004775435.1: 53,982-131,440 TSPEAR, KRTAP10-4, 7 more genes
    nsv5977718insertion1nstd209human GRCh38 chr21: 44,592,514-44,592,514 , GRCh37.p13 chr21|NW_004775435.1: 95,837-95,837 , GRCh37.p13 chr21: 46,012,395-46,012,395 TSPEAR, KRTAP10-6
    nsv5970889inversion1nstd209human GRCh38 chr21: 44,591,798-44,601,087 , GRCh37.p13 chr21: 46,011,679-46,021,002 , GRCh37.p13 chr21|NW_004775435.1: 95,121-104,410 TSPEAR, KRTAP10-6, 1 more genes
    nsv5966711copy number variation1nstd209human GRCh38 chr21: 44,682,494-44,682,876 , GRCh37.p13 chr21|NW_004775435.1: 185,815-186,197 , GRCh37.p13 chr21: 46,102,409-46,102,791 KRTAP12-1, TSPEAR
    nsv5966282copy number variation1nstd209human GRCh38 chr21: 44,511,290-44,511,350 , GRCh37.p13 chr21: 45,931,173-45,931,233 , GRCh37.p13 chr21|NW_004775435.1: 14,613-14,673 TSPEAR, TSPEAR-AS1
    nsv5966174copy number variation1nstd209human GRCh38 chr21: 44,523,488-44,524,180 , GRCh37.p13 chr21: 45,943,371-45,944,063 , GRCh37.p13 chr21|NW_004775435.1: 26,811-27,503 TSPEAR
    nsv5964338copy number variation1nstd209human GRCh38 chr21: 44,530,246-44,530,337 , GRCh37.p13 chr21|NW_004775435.1: 33,569-33,660 , GRCh37.p13 chr21: 45,950,129-45,950,220 TSPEAR
    nsv5964223copy number variation1nstd209human GRCh38 chr21: 44,696,977-44,697,095 , GRCh37.p13 chr21|NW_004775435.1: 200,298-200,416 , GRCh37.p13 chr21: 46,116,892-46,117,010 KRTAP10-12, TSPEAR
    nsv5962376copy number variation1nstd209human GRCh38 chr21: 44,502,910-44,503,000 , GRCh37.p13 chr21|NW_004775435.1: 6,233-6,323 , GRCh37.p13 chr21: 45,922,793-45,922,883 TSPEAR
    nsv5961461copy number variation1nstd209human GRCh38 chr21: 44,530,415-44,530,470 , GRCh37.p13 chr21|NW_004775435.1: 33,738-33,793 , GRCh37.p13 chr21: 45,950,298-45,950,353 TSPEAR
    nsv5960497copy number variation1nstd209human GRCh38 chr21: 44,574,464-44,574,730 , GRCh37.p13 chr21: 45,994,341-45,994,607 , GRCh37.p13 chr21|NW_004775435.1: 77,787-78,053 TSPEAR, KRTAP10-4
    nsv5960065copy number variation1nstd209human GRCh38 chr21: 44,574,107-44,574,730 , GRCh37.p13 chr21|NW_004775435.1: 77,430-78,053 , GRCh37.p13 chr21: 45,993,984-45,994,607 KRTAP10-4, TSPEAR
    nsv5959224copy number variation1nstd209human GRCh38 chr21: 44,504,438-44,504,672 , GRCh37.p13 chr21|NW_004775435.1: 7,761-7,995 , GRCh37.p13 chr21: 45,924,321-45,924,555 TSPEAR-AS1, TSPEAR
    nsv5958966copy number variation1nstd209human GRCh38 chr21: 44,627,404-44,627,526 , GRCh37.p13 chr21|NW_004775435.1: 130,727-130,849 , GRCh37.p13 chr21: 46,047,321-46,047,443 TSPEAR, KRTAP10-9
    nsv5957800copy number variation1nstd209human GRCh38 chr21: 44,539,504-44,539,644 , GRCh37.p13 chr21|NW_004775435.1: 42,827-42,967 , GRCh37.p13 chr21: 45,959,387-45,959,527 TSPEAR, KRTAP10-1
    nsv5955372copy number variation1nstd209human GRCh38 chr21: 44,523,072-44,523,159 , GRCh37.p13 chr21|NW_004775435.1: 26,395-26,482 , GRCh37.p13 chr21: 45,942,955-45,943,042 TSPEAR
    nsv5955074copy number variation1nstd209human GRCh38 chr21: 44,504,080-44,504,173 , GRCh37.p13 chr21|NW_004775435.1: 7,403-7,496 , GRCh37.p13 chr21: 45,923,963-45,924,056 TSPEAR, TSPEAR-AS1
    nsv5954604copy number variation1nstd209human GRCh38 chr21: 44,533,419-44,533,480 , GRCh37.p13 chr21|NW_004775435.1: 36,742-36,803 , GRCh37.p13 chr21: 45,953,302-45,953,363 TSPEAR
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