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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097530copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,007,858-34,008,124 , GRCh38.p12 chr5: 34,007,753-34,008,019 AMACR, C1QTNF3-AMACR
    nsv7097140copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,986,409-33,989,627 , GRCh38.p12 chr5: 33,986,304-33,989,522 C1QTNF3-AMACR, AMACR
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7093341copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,985,092-33,985,179 , GRCh38 chr5: 33,984,987-33,985,074 C1QTNF3-AMACR, AMACR, 1 more genes
    nsv7052596inversion1nstd229human GRCh38 chr5: 33,502,543-34,969,892 , GRCh37.p13 chr5: 33,502,648-34,969,997 TTC23L, DNAJC21, 22 more genes
    nsv7044635inversion1nstd229human GRCh38 chr5: 33,992,774-33,992,884 , GRCh37.p13 chr5: 33,992,879-33,992,989 C1QTNF3-AMACR, AMACR
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv6772121copy number variation1nstd229human GRCh38 chr5: 33,991,758-33,994,195 , GRCh37.p13 chr5: 33,991,863-33,994,300 C1QTNF3-AMACR, AMACR
    nsv6768447copy number variation1nstd229human GRCh38 chr5: 33,983,112-33,988,275 , GRCh37.p13 chr5: 33,983,217-33,988,380 SLC45A2, AMACR, 1 more genes
    nsv6764693copy number variation1nstd229human GRCh38 chr5: 33,302,234-34,039,432 , GRCh37.p13 chr5: 33,302,340-34,039,537 TARS1, SLC45A2, 12 more genes
    nsv6763595copy number variation1nstd229human GRCh38 chr5: 33,944,271-34,753,712 , GRCh37.p13 chr5: 33,944,376-34,753,817 RAI14-DT, C1QTNF3, 10 more genes
    nsv6758548copy number variation1nstd229human GRCh38 chr5: 34,004,897-34,007,482 , GRCh37.p13 chr5: 34,005,002-34,007,587 AMACR, C1QTNF3-AMACR
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630400copy number variation1nstd224human GRCh37 chr5: 33,909,843-34,028,972 , GRCh38.p12 chr5: 33,909,738-34,028,867 AMACR, SLC45A2, 4 more genes
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6569683inversion1nstd223human GRCh38 chr5: 33,993,610-33,994,342 , GRCh37.p13 chr5: 33,993,715-33,994,447 C1QTNF3-AMACR, AMACR
    nsv6392558copy number variation1nstd223human GRCh38 chr5: 33,985,585-33,986,027 , GRCh37.p13 chr5: 33,985,690-33,986,132 C1QTNF3-AMACR, AMACR
    nsv6391227copy number variation1nstd223human GRCh38 chr5: 33,991,378-33,993,705 , GRCh37.p13 chr5: 33,991,483-33,993,810 C1QTNF3-AMACR, AMACR
    nsv6380333copy number variation1nstd223human GRCh38 chr5: 33,944,257-34,753,777 , GRCh37.p13 chr5: 33,944,362-34,753,882 GUSBP18, RAI14-DT, 10 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
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