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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
    nsv6636011copy number variation1nstd102humanUncertain significance GRCh37 chrY: 3,182,436-4,765,099 , GRCh38.p12 chrY: 3,314,395-4,897,058 USP12PY, MIR9985, 8 more genes
    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
    nsv6315264copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,114,097 , GRCh38.p12 chrY: 2,782,099-7,246,056 RNU6-1334P, SRIP3, 50 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
    nsv6290512copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,054,478-3,476,941 , GRCh38.p12 chrY: 3,186,437-3,608,900 AGPAT5P1, TGIF2LY, 1 more genes
    nsv6290500copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,037,425-5,670,611 , GRCh38.p12 chrY: 3,169,384-5,802,570 EIF4A1P2, RNU6-303P, 16 more genes
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5431133copy number variation1nstd206human GRCh38 chrY: 2,781,388-3,953,388 , GRCh37.p13 chrY: 2,649,429-3,821,429 UBE2V1P3, LOC105377227, 17 more genes
    nsv4909309copy number variation1nstd200human GRCh38 chrY: 3,274,144-3,590,456 , GRCh37.p13 chrY: 3,142,185-3,458,497 AGPAT5P1, PRRC2CP1, 1 more genes
    nsv4728396copy number variation1nstd102humanUncertain significance GRCh37 chrY: 3,147,902-3,476,941 , GRCh38.p12 chrY: 3,279,861-3,608,900 TGIF2LY, AGPAT5P1, 1 more genes
    nsv4728217copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,069,286-5,727,224 , GRCh38.p12 chrY: 3,201,245-5,859,183 SERBP1P2, RNU2-57P, 16 more genes
    nsv4684048copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-6,367,818 , GRCh38.p12 chrY: 2,782,099-6,499,777 SNX3P1Y, LOC100533723, 42 more genes
    nsv4684046copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-7,019,586 , GRCh38.p12 chrY: 2,782,099-7,151,545 KRT18P10, TTTY23B, 50 more genes
    nsv4684040copy number variation1nstd102humanPathogenic GRCh37 chrY: 2,650,140-6,172,892 , GRCh38.p12 chrY: 2,782,099-6,304,851 ZFY, TGIF2LY, 34 more genes
    nsv4674653copy number variation1nstd102humanLikely benign GRCh37 chrY: 3,037,424-5,739,448 , GRCh38.p12 chrY: 3,169,383-5,871,407 SERBP1P2, SNX3P1Y, 16 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
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