dbVar for Gene (Select 101927727) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	RFLNB, C17orf100, 401 more genes
nsv7098743	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802	PAFAH1B1, RN7SL33P, 65 more genes
nsv7098729	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857	MYO1C, SERPINF1, 42 more genes
nsv7094896	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446	SLC43A2, LOC105371480, 34 more genes
nsv7077982	inversion	1	nstd229	human		GRCh38 chr17: 662,447-915,193 , GRCh37.p13 chr17: 565,687-818,433	GLOD4, LOC101927727, 6 more genes
nsv7077625	inversion	1	nstd229	human		GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981	MIR3183, YWHAE, 75 more genes
nsv7074008	inversion	1	nstd229	human		GRCh38 chr17: 792,423-988,811 , GRCh37.p13 chr17: 695,663-892,051	NXN, LOC101927727, 1 more genes
nsv7060173	inversion	1	nstd229	human		GRCh38 chr17: 810,439-918,493 , GRCh37.p13 chr17: 713,679-821,733	LOC101927727, NXN
nsv6997473	copy number variation	1	nstd229	human		GRCh38 chr17: 814,252-951,344 , GRCh37.p13 chr17: 717,492-854,584	NXN, LOC101927727
nsv6997370	copy number variation	1	nstd229	human		GRCh38 chr17: 879,121-954,338 , GRCh37.p13 chr17: 782,361-857,578	LOC101927727, NXN
nsv6995849	copy number variation	1	nstd229	human		GRCh38 chr17: 426,628-969,586 , GRCh37.p13 chr17: 396,627-872,826	VPS53, MRM3, 8 more genes
nsv6994867	copy number variation	1	nstd229	human		GRCh38 chr17: 856,745-1,043,814 , GRCh37.p13 chr17: 759,985-947,054	NXN, ABR, 4 more genes
nsv6991988	copy number variation	1	nstd229	human		GRCh38 chr17: 251,815-1,065,942 , GRCh37.p13 chr17: 396,627-969,182	LIAT1, RPS4XP17, 17 more genes
nsv6990292	copy number variation	1	nstd229	human		GRCh38 chr17: 835,113-993,236 , GRCh37.p13 chr17: 738,353-896,476	LOC101927727, NXN
nsv6988554	copy number variation	1	nstd229	human		GRCh38 chr17: 301,576-970,376 , GRCh37.p13 chr17: 396,627-873,616	RPS4XP17, RFLNB, 13 more genes
nsv6983504	copy number variation	1	nstd229	human		GRCh38 chr17: 834,665-915,215 , GRCh37.p13 chr17: 737,905-818,455	LOC101927727, NXN
nsv6981473	copy number variation	1	nstd229	human		GRCh38 chr17: 903,601-912,300 , GRCh37.p13 chr17: 806,841-815,540	NXN, LOC101927727
nsv6637994	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 735,868-858,326 , GRCh38.p12 chr17: 832,628-955,086	LOC101927727, NXN
nsv6637807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 489,311-831,589 , GRCh38.p12 chr17: 586,071-928,349	LOC101927727, VPS53, 7 more genes
nsv6637614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 665,031-831,589 , GRCh38.p12 chr17: 761,791-928,349	NXN, LOC101927727, 2 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 380

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Number of Variants: 20

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