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Items: 1 to 20 of 294

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634344copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-9,651,417 , GRCh38.p12 chrY: 2,782,099-9,813,808 LOC105377235, TTTY7B, 135 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315229copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 RBMY2VP, RFTN1P1, 570 more genes
    nsv6314745copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,424-28,799,654 , GRCh38.p12 chrY: 2,782,383-26,653,507 TTTY20, USP9YP18, 524 more genes
    nsv6290416copy number variation1nstd102humanLikely benign GRCh37 chrY: 9,200,031-9,381,164 , GRCh38.p12 chrY: 9,362,422-9,543,555 TSPY6P, FAM197Y5, 10 more genes
    nsv6290378copy number variation1nstd102humanUncertain significance GRCh37 chrY: 9,172,547-9,376,012 , GRCh38.p12 chrY: 9,334,938-9,538,403 FAM197Y7, TSPY3, 14 more genes
    nsv6137420copy number variation1nstd213human GRCh37 chrY: 8,710,000-9,320,001 , GRCh38.p12 chrY: 8,841,959-9,482,392 TSPY1, RBMY2MP, 23 more genes
    nsv5671934copy number variation1nstd207human GRCh38 chrY: 9,361,810-9,552,074 , GRCh37.p13 chrY: 9,199,419-9,389,683 TSPY6P, TSPY10, 11 more genes
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5423876copy number variation1nstd206human GRCh38 chrY: 9,108,931-21,750,314 , GRCh37.p13 chrY: 8,964,956-23,901,428 , TSPY14P, 238 more genes
    nsv4730219inversion4nstd198human GRCh38 chrY: 6,198,014-9,936,872 , GRCh37.p13 chrY: 6,066,055-9,774,481 , AMELY, 109 more genes
    nsv4674267copy number variation1nstd102humanLikely benign GRCh37 chrY: 9,221,114-9,372,133 , GRCh38.p12 chrY: 9,383,505-9,534,524 FAM197Y3, TSPY10, 8 more genes
    nsv4674211copy number variation1nstd102humanLikely benign GRCh37 chrY: 9,168,143-9,372,133 , GRCh38.p12 chrY: 9,330,534-9,534,524 FAM197Y8, FAM197Y2, 15 more genes
    nsv4673949copy number variation1nstd102humanPathogenic GRCh37 chrY: 168,546-28,799,937 , GRCh38.p12 chrY: 301,879-26,653,790 GPM6BP2, TTTY18, 559 more genes
    nsv4673928copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-16,095,773 , GRCh38.p12 chrY: 10,001-13,983,893 TTTY21, MTCO3P37, 239 more genes
    nsv4640346copy number variation4nstd186human GRCh37 chrY: 9,291,322-9,332,500 , GRCh38.p12 chrY: 9,453,714-9,494,891 TSPY1, TSPY9, 2 more genes
    nsv4454174copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-20,619,847 , GRCh38.p12 chrY: 2,782,099-18,457,961 ZNF736P8Y, FAM197Y7, 269 more genes
    nsv4451989copy number variation1nstd102humanPathogenic GRCh37 chrY: 118,546-20,603,124 , GRCh38.p12 chrY: 251,879-18,441,238 LOC107985677, SOWAHCP1, 303 more genes
    nsv4451304copy number variation1nstd102humanPathogenic GRCh37 chrY: 201,704-15,182,563 , GRCh38.p12 chrY: 320,650-13,070,649 NAP1L1P2, AGPAT5P1, 226 more genes
    nsv4385524copy number variation3nstd173human GRCh37 chrY: 2,650,141-28,799,949 , GRCh38.p12 chrY: 2,782,100-26,653,802 , MTND1P12, 527 more genes
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