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Items: 1 to 20 of 563

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056651inversion1nstd229human GRCh38 chr2: 174,826,021-174,826,317 , GRCh37.p13 chr2: 175,690,749-175,691,045 CHN1
    nsv7049124inversion1nstd229human GRCh38 chr2: 174,401,435-175,981,960 , GRCh37.p13 chr2: 175,266,163-176,846,688 LNPK, RNU7-44P, 19 more genes
    nsv7047218inversion1nstd229human GRCh38 chr2: 174,808,649-174,813,816 , GRCh37.p13 chr2: 175,673,377-175,678,544 CHN1
    nsv7044829inversion1nstd229human GRCh38 chr2: 174,961,568-174,961,681 , GRCh37.p13 chr2: 175,826,296-175,826,409 CHN1
    nsv7042192inversion1nstd229human GRCh38 chr2: 174,830,361-174,836,573 , GRCh37.p13 chr2: 175,695,089-175,701,301 CHN1
    nsv7039194inversion1nstd229human GRCh38 chr2: 174,826,092-174,826,412 , GRCh37.p13 chr2: 175,690,820-175,691,140 CHN1
    nsv6697949copy number variation1nstd229human GRCh38 chr2: 174,861,842-174,865,807 , GRCh37.p13 chr2: 175,726,570-175,730,535 CHN1
    nsv6697926copy number variation1nstd229human GRCh38 chr2: 174,973,460-174,974,814 , GRCh37.p13 chr2: 175,838,188-175,839,542 CHN1
    nsv6695846copy number variation1nstd229human GRCh38 chr2: 174,845,816-174,845,916 , GRCh37.p13 chr2: 175,710,544-175,710,644 CHN1
    nsv6695834copy number variation1nstd229human GRCh38 chr2: 174,993,037-175,003,655 , GRCh37.p13 chr2: 175,857,765-175,868,383 CHN1
    nsv6694690copy number variation1nstd229human GRCh38 chr2: 174,903,020-174,911,708 , GRCh37.p13 chr2: 175,767,748-175,776,436 CHN1
    nsv6691982copy number variation1nstd229human GRCh38 chr2: 174,819,192-174,830,502 , GRCh37.p13 chr2: 175,683,920-175,695,230 CHN1
    nsv6691816copy number variation1nstd229human GRCh38 chr2: 174,974,211-174,987,411 , GRCh37.p13 chr2: 175,838,939-175,852,139 CHN1
    nsv6691799copy number variation1nstd229human GRCh38 chr2: 174,951,963-174,960,017 , GRCh37.p13 chr2: 175,816,691-175,824,745 CHN1
    nsv6690667copy number variation1nstd229human GRCh38 chr2: 174,799,101-174,799,285 , GRCh37.p13 chr2: 175,663,829-175,664,013 CHN1
    nsv6689760copy number variation1nstd229human GRCh38 chr2: 174,890,513-174,895,015 , GRCh37.p13 chr2: 175,755,241-175,759,743 CHN1
    nsv6688648copy number variation1nstd229human GRCh38 chr2: 174,962,716-174,971,166 , GRCh37.p13 chr2: 175,827,444-175,835,894 CHN1
    nsv6687139copy number variation1nstd229human GRCh38 chr2: 174,949,201-174,951,200 , GRCh37.p13 chr2: 175,813,929-175,815,928 CHN1
    nsv6686922copy number variation1nstd229human GRCh38 chr2: 174,807,418-174,808,842 , GRCh37.p13 chr2: 175,672,146-175,673,570 CHN1
    nsv6683794copy number variation1nstd229human GRCh38 chr2: 175,005,478-175,027,416 , GRCh37.p13 chr2: 175,870,206-175,892,144 RNU6-763P, CHN1
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